510(k) Report

510(k) · Cleared

Recalled · Class II · 2021

Trinity Non-Occluded Titanium Plasma Sprayed (TPS) Acetabular Shells

K123705510(k) TraditionalCleared Feb 12, 201371-day reviewClass II21 CFR 888.3353Recalls 4

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Corin USA · LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

Cleared on Feb 12, 2013 as substantially equivalent to K093472 (Corin USA, 2010) and 3 other predicates after a 71-day review. Its family tree reaches back 12 generations to 1981. 23 later devices descend from it. It has been recalled 4 times.

Decided
Feb 12, 2013
Review
71 days
Class
Class II
Product code
LZO
Recalls
4
Predicates
4

Its longest line of descent runs back 12 generations to K810258 (1981). 100 ancestors in all. 23 later devices descend from it, 4 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2010: 1 other ancestor2005: 3 other ancestors2009: 2 other ancestors2004: 6 other ancestors2003: 3 other ancestors2001: 6 other ancestors2000: 12 other ancestors1999: 4 other ancestors2002: 8 other ancestors1997: 6 other ancestors1996: 5 other ancestors1994: 11 other ancestors2006: 1 other ancestor1998: 3 other ancestors1995: 6 other ancestors1993: 2 other ancestors1991: 2 other ancestors1990: 1 other ancestor1984: 1 other ancestor1992: 2 other ancestors1987: 1 other ancestor1985: 1 other ancestor2016: 2 descendants cleared2015: 1 descendant cleared2021: 3 descendants cleared2019: 4 descendants cleared2018: 1 descendant cleared2020: 5 descendants cleared2023: 1 descendant cleared2024: 2 descendants cleared2026: 2 descendants cleared2022: 1 descendant cleared2025: 1 descendant clearedK810258 · Proximal Fermoral Hip Replacement · Biomet, Inc. · 1981K974558 · Salvage/Onocology Hip and Total Femur System · Biomet, Inc. · 1998K032396 · Ringloc 36MM Line and Modular Femoral Heads · Biomet, Inc. · 2003 · recalled×2: 2 generations cleared close together, K042051 (2005), K051411 (2005) K061312 · 36MM Biolox Delta Ceramic Heads · Biomet, Inc. · 2006K071535 · Biolox Delta Ceramic Femoral Head · Zimmer, Inc. · 2007 · recalledK082844 · Biolox Delta Ceramic Femoral Head, Biolox Delta Ceramic Femoral Head Offset Sleeve · Encore Medical L.P. · 2008 · recalledK100412 · Biolox Delta Ceramic Femoral Heads · Smith & Nephew, Inc. · 2010×2: 2 generations cleared close together, K103120 (2011), K110087 (2011) K122305 · Corin Trinity-I Acetabular Shell · Corin USA · 201219801990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 2 other ancestors2 generations back: 12 other ancestors3 generations back: 15 other ancestors4 generations back: 14 other ancestors5 generations back: 21 other ancestors6 generations back: 10 other ancestors7 generations back: 11 other ancestors8 generations back: 2 other ancestors 1 generation forward: 4 descendants2 generations forward: 11 descendants3 generations forward: 6 descendants4 generations forward: 2 descendants K122305 · Corin Trinity-I Acetabular Shell · Corin USA · 2012K110087 · Corin Trinity Acetbular System with Hxlpe Liners · Corin USA · 2011K103120 · Corin Biolox Delta Femoral Heads · Corin USA · 2011K100412 · Biolox Delta Ceramic Femoral Heads · Smith & Nephew, Inc. · 2010K082844 · Biolox Delta Ceramic Femoral Head, Biolox Delta Ceramic Femoral Head Offset Sleeve · Encore Medical L.P. · 2008 · recalledK071535 · Biolox Delta Ceramic Femoral Head · Zimmer, Inc. · 2007 · recalledK061312 · 36MM Biolox Delta Ceramic Heads · Biomet, Inc. · 2006K051411 · Arcomxl Polyethylene Liners and Biolox Delta Heads · Biomet, Inc. · 2005 · recalledK042051 · Arcomxl Polyethylene Liners · Biomet, Inc. · 2005 · recalledK032396 · Ringloc 36MM Line and Modular Femoral Heads · Biomet, Inc. · 2003 · recalledK974558 · Salvage/Onocology Hip and Total Femur System · Biomet, Inc. · 1998K810258 · Proximal Fermoral Hip Replacement · Biomet, Inc. · 1981−10−50
  1. Root · 12 generations backK810258 Proximal Fermoral Hip ReplacementBiomet, Inc. · 1981
  2. 8 generations between
  3. 3 generations backK103120 Corin Biolox Delta Femoral HeadsCorin USA · 2011
  4. 2 generations backK110087 Corin Trinity Acetbular System with Hxlpe LinersCorin USA · 2011
  5. 1 generation backK122305 Corin Trinity-I Acetabular ShellCorin USA · 2012
  6. This deviceK123705 Trinity Non-Occluded Titanium Plasma Sprayed (TPS) Acetabular ShellsCorin USA · 2013
  7. Descendant · cites it directly · 8 of its ownK182321 MobileLink Acetabular Cup SystemWaldemar Link GmbH & Co. KG · 2019
  8. Descendant · cites it directly · 8 of its ownK152893 Corin Optimized Positioning System (OPS)Corin USA · 2016
  9. Descendant · 2 generations on · 5 of its ownK190834 Corin Optimized Position System Functional Hip Analysis (OPS FHA)Corin USA · 2019
  10. Descendant · 2 generations on · 4 of its ownK192559 Acetabular Bone Screws (for MobileLink Acetabular Cup System)Waldemar Link GmbH & Co. KG · 2019
  11. Descendant · cites it directly · 4 of its ownK142761 Corin TaperFit Hip StemCorin USA · 2015 · Recalled
Show all 12 generations
  1. Root · 12 generations backK810258 Proximal Fermoral Hip ReplacementBiomet, Inc. · 1981
  2. 11 generations backK974558 Salvage/Onocology Hip and Total Femur SystemBiomet, Inc. · 1998
  3. 10 generations backK032396 Ringloc 36MM Line and Modular Femoral HeadsBiomet, Inc. · 2003 · Recalled
  4. 9 generations backK042051 Arcomxl Polyethylene LinersBiomet, Inc. · 2005 · Recalled
  5. 8 generations backK051411 Arcomxl Polyethylene Liners and Biolox Delta HeadsBiomet, Inc. · 2005 · Recalled
  6. 7 generations backK061312 36MM Biolox Delta Ceramic HeadsBiomet, Inc. · 2006
  7. 6 generations backK071535 Biolox Delta Ceramic Femoral HeadZimmer, Inc. · 2007 · Recalled
  8. 5 generations backK082844 Biolox Delta Ceramic Femoral Head, Biolox Delta Ceramic Femoral Head…Encore Medical L.P. · 2008 · Recalled
  9. 4 generations backK100412 Biolox Delta Ceramic Femoral HeadsSmith & Nephew, Inc. · 2010
  10. 3 generations backK103120 Corin Biolox Delta Femoral HeadsCorin USA · 2011
  11. 2 generations backK110087 Corin Trinity Acetbular System with Hxlpe LinersCorin USA · 2011
  12. 1 generation backK122305 Corin Trinity-I Acetabular ShellCorin USA · 2012
  13. This deviceK123705 Trinity Non-Occluded Titanium Plasma Sprayed (TPS) Acetabular ShellsCorin USA · 2013

Showing 5 of 23 descendants. See all descendants

Descendants cleared per year

2015: 12016: 22018: 12019: 42020: 52021: 32022: 12023: 12024: 22025: 12026: 2
2015high 5 (2020) · low 0 (2017)2026

Most influential descendants

Showing 5 of 23 · See all
  • K182321MobileLink Acetabular Cup SystemWaldemar Link GmbH & Co. KG · 2019 · cites it directly8descendants
  • K152893Corin Optimized Positioning System (OPS)Corin USA · 2016 · cites it directly8descendants
  • K190834Corin Optimized Position System Functional Hip Analysis (OPS FHA)Corin USA · 2019 · 2 generations on5descendants
  • K192559Acetabular Bone Screws (for MobileLink Acetabular Cup System)Waldemar Link GmbH & Co. KG · 2019 · 2 generations on4descendants
  • K142761Corin TaperFit Hip StemCorin USA · 2015 · cites it directly4descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−12K810258Proximal Fermoral Hip ReplacementBiomet, Inc.1981—
−11K974558Salvage/Onocology Hip and Total Femur SystemBiomet, Inc.1998—
−10K032396Ringloc 36MM Line and Modular Femoral HeadsBiomet, Inc.20033
−9K042051Arcomxl Polyethylene LinersBiomet, Inc.20051
−8K051411Arcomxl Polyethylene Liners and Biolox Delta HeadsBiomet, Inc.20051
−7K06131236MM Biolox Delta Ceramic HeadsBiomet, Inc.2006—
−6K071535Biolox Delta Ceramic Femoral HeadZimmer, Inc.20073
−5K082844Biolox Delta Ceramic Femoral Head, Biolox Delta Ceramic Femoral Head Offset…Encore Medical L.P.20081
−4K100412Biolox Delta Ceramic Femoral HeadsSmith & Nephew, Inc.2010—
−3K103120Corin Biolox Delta Femoral HeadsCorin USA2011—
−2K110087Corin Trinity Acetbular System with Hxlpe LinersCorin USA2011—
−1K122305Corin Trinity-I Acetabular ShellCorin USA2012—
0 (this device)K123705Trinity Non-Occluded Titanium Plasma Sprayed (TPS) Acetabular ShellsCorin USA2013—
+1K182321MobileLink Acetabular Cup SystemWaldemar Link GmbH & Co. KG2019—
+1K152893Corin Optimized Positioning System (OPS)Corin USA2016—
+2K190834Corin Optimized Position System Functional Hip Analysis (OPS FHA)Corin USA2019—
+2K192559Acetabular Bone Screws (for MobileLink Acetabular Cup System)Waldemar Link GmbH & Co. KG2019—
+1K142761Corin TaperFit Hip StemCorin USA20151

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198410
198510
198710
199010
199120
199220
199320
1994110
199560
199650
199760
199830
199940
2000120
200160
200280
200330
200460
200530
200610
200920
201010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201510
201620
201810
201940
202050
202130
202210
202310
202420
202510
202620
FIG. 1 — Lineage of K123705, 1981–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in LZO? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new LZO device

  1. #1 K192827 Quadra-Pscore 19.3 · 10 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (4)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K093472Trinity Acetabular System
Summary page 2
…of Technologies /Sub3stantial Equivalence: The standard Trinity Non-occluded TPS shell is identical to the standard Trinity Acetabular Shell cleared in K093472 and K1 10087 in terms of intended use, indications for use, substrate materials, and size range. Likewise, the 'Trinity-…
Corin USA20101
*K110087Corin Trinity Acetbular System with Hxlpe Liners
Summary page 1
…. Legally Marketed Devices to which Substantial Equivalence is claimed: a. Corin Trinity Acetabular System (K(093472) b. Corin Trinity Acetabular System with HXLPE (K1 10087) c. Corin Trinity Acetabular System with Trinity-i Acetabular Shells (K122305) d. United U32 Acetabular Component (K(050262)…
Corin USA2011—
*K122305Corin Trinity-I Acetabular Shell
Summary page 1
…n Trinity Acetabular System (K(093472) b. Corin Trinity Acetabular System with HXLPE (K1 10087) c. Corin Trinity Acetabular System with Trinity-i Acetabular Shells (K122305) d. United U32 Acetabular Component (K(050262) 7. Device Description: The Trinity Acetabular System is a modular aceta…
Corin USA2012—
*K050262U2 Acetabular Component
Summary page 1
…Trinity Acetabular System with HXLPE (K1 10087) c. Corin Trinity Acetabular System with Trinity-i Acetabular Shells (K122305) d. United U32 Acetabular Component (K(050262) 7. Device Description: The Trinity Acetabular System is a modular acetabular cup system consisting of a press…
United Orthopedic Corp.2005—

Also cleared against K093472: 18 other devices →

What descends from it? (23)

See all 23

4 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K182321MobileLink Acetabular Cup SystemWaldemar Link GmbH & Co. KG20198
K152893Corin Optimized Positioning System (OPS)Corin USA20168
K142761Corin TaperFit Hip StemCorin USA20154
K201657Corin Ltd. Hip Products: Trinity™ Acetabular System, Trinity™ PLUS Acetabular Shell…Corin, Ltd.20212

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Jul 28, 2021Class IIZ-2605-2021StorageThe packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices.
Jan 29, 2016Class IIZ-1528-2016Packaging process controlPotential for abrasion of the sterile barrier pouches of the new packaging system.
Jan 29, 2016Class IIZ-1527-2016Packaging process controlPotential for abrasion of the sterile barrier pouches of the new packaging system.
Jan 29, 2016Class IIZ-1526-2016Packaging process controlPotential for abrasion of the sterile barrier pouches of the new packaging system.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 32 years and passes through 5 companies; a new generation was cleared every 1.4 years on median.
  • 26 of the 99 ancestors have a recall of any class.
  • Of its descendants, K182321 (Waldemar Link GmbH & Co. KG, 2019) has gone furthest, with 8 descendants of its own.
  • 18 other devices also cite its predicate K093472.

How does its category compare?

All LZO devices

LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.

FDA decisions per year · LZO

14in 2025

2007: 92008: 112009: 72010: 152011: 132012: 142013: 262014: 132015: 122016: 102017: 162018: 182019: 282020: 182021: 122022: 112023: 102024: 112025: 142026 (partial year): 9
2007high 28 (2019) · low 7 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LZO

119in 2025

2007: 87 days median2008: 63 days median2009: 83 days median2010: 78 days median2011: 87 days median2012: 98 days median2013: 100 days median2014: 85 days median2015: 115 days median2016: 177 days median2017: 257 days median2018: 163 days median2019: 109 days median2020: 112 days median2021: 170 days median2022: 279 days median2023: 122 days median2024: 111 days median2025: 119 days median2026 (partial year): 102 days median
2007high 279 (2022) · low 63 (2008)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · LZO

1in 2025

2007: 22008: 132009: 422011: 102012: 142014: 12015: 12016: 92017: 52018: 22019: 42020: 32022: 42023: 22024: 12025: 1
2007high 42 (2009) · low 0 (2010)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · LZO

3,244in 2025

2007: 1382008: 1252009: 1892010: 3942011: 5442012: 9632013: 1,3702014: 1,4772015: 1,3482016: 1,7282017: 2,1652018: 3,1332019: 3,0662020: 1,9632021: 2,1992022: 1,9852023: 2,0662024: 2,5862025: 3,244
2007high 3,244 (2025) · low 125 (2008)2025

MAUDE reports naming product code LZO, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20079872138
2008116313125
200978342189
201015780394
2011138710544
2012149814963
20132610001,370
2014138511,477
20151211511,348
20161017791,728
20171625752,165
20181816323,133
20192810943,066
20201811231,963
20211217002,199
20221127941,985
20231012222,066
20241111112,586
20251411913,244
202691020—

What is it indicated for?

The indications for the Trinity Acetabular System as a total hip arthroplastv include:

Non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis

Rheumatoid arthritis

Correction of functional deformity

Developmental dysplasia of the hip (DDIt or congenital dlysplasia of the hip (CDH)

The Trinity Acetabular System is indicated for cementless, single use only.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K123705: Trinity Non-Occluded Titanium Plasma Sprayed (TPS) Acetabular Shells.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K123705

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026