510(k) Report

510(k) · Cleared

Cleared

Straumann Cares Screw-Retained Bridge Titanium, Straumann Cares Dolder Bar Titanium

K112280510(k) SpecialCleared Nov 16, 201199-day reviewClass II21 CFR 872.3630

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

Straumann USA · NHA Abutment, Implant, Dental, Endosseous

Cleared on Nov 16, 2011 as substantially equivalent to K101465 (Institut Straumann AG, 2010) after a 99-day review. Its family tree reaches back 12 generations to 1990.

Decided
Nov 16, 2011
Review
99 days
Class
Class II
Product code
NHA
Recalls
None
Predicates
1

Its longest line of descent runs back 12 generations to K894844 (1990). 77 ancestors in all, the oldest K871863 (1987). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2009: 1 other ancestor2004: 4 other ancestors2008: 1 other ancestor2006: 2 other ancestors2002: 4 other ancestors1996: 8 other ancestors2005: 1 other ancestor2001: 4 other ancestors2000: 2 other ancestors1998: 3 other ancestors1995: 7 other ancestors1999: 3 other ancestors1997: 3 other ancestors1994: 9 other ancestors1989: 1 other ancestor1987: 1 other ancestor1993: 9 other ancestors1990: 1 other ancestor1991: 1 other ancestorK894844 · Bonefit Implant System Accessories & Instruments · Straumann Institute, Ltd. · 1990K990342 · Synocta Prosthetics · Straumann USA · 1999×2: 2 generations cleared close together, K013798 (2001), K020096 (2002) K033243 · Iti Synocta Meso Abutments · Straumann USA · 2003K052272 · Straumann Computer Aided Restoration Service · Straumann USA · 2006K061277 · Straumann Computer Aided Restoration Service (C.a.R.E.S.) Ceramic Coping · Straumann USA · 2007K072151 · P.004 RC Cares Titanium and Ceramic Abutments · Straumann USA · 2007 · recalledK081005 · P.004 NC Cares Titanium and Ceramic Abutments · Institut Straumann AG · 2008 · recalledK082545 · Straumann NN Cares Titanium and Ceramic Abutments · Institut Straumann AG · 2008K093113 · Etkon ES1, Model 019.0001, Etkon Visual, Straumann Cadcam Abutment · Institut Straumann AG · 2009K101465 · Straumann Cares Bridge; Straumann Cares Dolder Bar · Institut Straumann AG · 2010198519901995200020052010
  1. Root · 12 generations backK894844 Bonefit Implant System Accessories & InstrumentsStraumann Institute, Ltd. · 1990
  2. 8 generations between
  3. 3 generations backK082545 Straumann NN Cares Titanium and Ceramic AbutmentsInstitut Straumann AG · 2008
  4. 2 generations backK093113 Etkon ES1, Model 019.0001, Etkon Visual, Straumann Cadcam AbutmentInstitut Straumann AG · 2009
  5. 1 generation backK101465 Straumann Cares Bridge; Straumann Cares Dolder BarInstitut Straumann AG · 2010
  6. This deviceK112280 Straumann Cares Screw-Retained Bridge Titanium, Straumann Cares…Straumann USA · 2011
Show all 12 generations
  1. Root · 12 generations backK894844 Bonefit Implant System Accessories & InstrumentsStraumann Institute, Ltd. · 1990
  2. 11 generations backK990342 Synocta ProstheticsStraumann USA · 1999
  3. 10 generations backK013798 Prosthetic Accessories to the Iti Dental Implant SystemInstitut Straumann AG · 2001
  4. 9 generations backK020096 Esthetic Ease Abutments for the Iti Dental Implant SystemInstitut Straumann AG · 2002 · Recalled
  5. 8 generations backK033243 Iti Synocta Meso AbutmentsStraumann USA · 2003
  6. 7 generations backK052272 Straumann Computer Aided Restoration ServiceStraumann USA · 2006
  7. 6 generations backK061277 Straumann Computer Aided Restoration Service (C.a.R.E.S.) Ceramic…Straumann USA · 2007
  8. 5 generations backK072151 P.004 RC Cares Titanium and Ceramic AbutmentsStraumann USA · 2007 · Recalled
  9. 4 generations backK081005 P.004 NC Cares Titanium and Ceramic AbutmentsInstitut Straumann AG · 2008 · Recalled
  10. 3 generations backK082545 Straumann NN Cares Titanium and Ceramic AbutmentsInstitut Straumann AG · 2008
  11. 2 generations backK093113 Etkon ES1, Model 019.0001, Etkon Visual, Straumann Cadcam AbutmentInstitut Straumann AG · 2009
  12. 1 generation backK101465 Straumann Cares Bridge; Straumann Cares Dolder BarInstitut Straumann AG · 2010
  13. This deviceK112280 Straumann Cares Screw-Retained Bridge Titanium, Straumann Cares…Straumann USA · 2011
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−12K894844Bonefit Implant System Accessories & InstrumentsStraumann Institute, Ltd.1990—
−11K990342Synocta ProstheticsStraumann USA1999—
−10K013798Prosthetic Accessories to the Iti Dental Implant SystemInstitut Straumann AG2001—
−9K020096Esthetic Ease Abutments for the Iti Dental Implant SystemInstitut Straumann AG20021
−8K033243Iti Synocta Meso AbutmentsStraumann USA2003—
−7K052272Straumann Computer Aided Restoration ServiceStraumann USA2006—
−6K061277Straumann Computer Aided Restoration Service (C.a.R.E.S.) Ceramic CopingStraumann USA2007—
−5K072151P.004 RC Cares Titanium and Ceramic AbutmentsStraumann USA20071
−4K081005P.004 NC Cares Titanium and Ceramic AbutmentsInstitut Straumann AG20081
−3K082545Straumann NN Cares Titanium and Ceramic AbutmentsInstitut Straumann AG2008—
−2K093113Etkon ES1, Model 019.0001, Etkon Visual, Straumann Cadcam AbutmentInstitut Straumann AG2009—
−1K101465Straumann Cares Bridge; Straumann Cares Dolder BarInstitut Straumann AG2010—
0 (this device)K112280Straumann Cares Screw-Retained Bridge Titanium, Straumann Cares Dolder Bar…Straumann USA2011—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198710
198910
199010
199110
199390
199490
199570
199680
199730
199830
199930
200020
200140
200240
200440
200510
200620
200810
200910
FIG. 1 — Lineage of K112280, 1990–2011Source: 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 NHA? 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 NHA device

  1. #1 K222288 DESS Dental Smart Solutionsscore 30.6 · 19 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? (1)

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
*K101465Straumann Cares Bridge; Straumann Cares Dolder Bar
Summary page 1
…Regulation Number: §872.3630 4. Legally Marketed Device to which Equivalence is Claimed (Predicate Device) K101465, Straumann® CARES® Screw-retained Bridge and Straumann® CARES® Dolder® Bar 5. Description of the Dev…
Institut Straumann AG2010—

Also cleared against K101465: 1 other device →

What descends from it?

No later submission names this one as a predicate yet.

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

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 21 years and passes through 3 companies; a new generation was cleared every 1.2 years on median.
  • 11 of the 77 ancestors have a recall of any class.
  • 1 other device also cites its predicate K101465.

How does its category compare?

All NHA devices

NHA Abutment, Implant, Dental, Endosseous: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.

FDA decisions per year · NHA

40in 2025

2007: 382008: 312009: 302010: 192011: 312012: 252013: 222014: 272015: 292016: 382017: 312018: 312019: 282020: 382021: 292022: 332023: 512024: 432025: 402026 (partial year): 23
2007high 51 (2023) · low 19 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NHA

147in 2025

2007: 91 days median2008: 90 days median2009: 95 days median2010: 162 days median2011: 130 days median2012: 171 days median2013: 184 days median2014: 160 days median2015: 151 days median2016: 202 days median2017: 188 days median2018: 200 days median2019: 160 days median2020: 153 days median2021: 211 days median2022: 142 days median2023: 147 days median2024: 158 days median2025: 147 days median2026 (partial year): 169 days median
2007high 211 (2021) · low 90 (2008)2026

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

Recalls per year · NHA

1in 2025

2007: 12008: 22011: 52012: 12013: 12015: 12016: 362017: 22018: 12020: 72023: 32025: 12026 (partial year): 3
2007high 36 (2016) · low 0 (2009)2026

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

Adverse event reports per year · NHA

838in 2025

2007: 12008: 82009: 302010: 612011: 562012: 52013: 1432014: 1462015: 8582016: 3142017: 5772018: 5912019: 5302020: 4582021: 5462022: 4972023: 6182024: 6352025: 838
2007high 858 (2015) · low 1 (2007)2025

MAUDE reports naming product code NHA, 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
2007389111
2008319028
20093095030
201019162061
201131130556
20122517115
2013221841143
2014271600146
2015291511858
20163820236314
2017311882577
2018312001591
2019281600530
2020381537458
2021292110546
2022331420497
2023511473618
2024431580635
2025401471838
2026231693—

What is it indicated for?

The Straumann® CARES® Screw-retained Bridge Titanium and Straumann® CARES® Dolder® Bar Titanium are indicated for use as bars and bridges that attach to dental implants (Straumann Regular Neck (RN) 04.8mm and Wide Neck (WN) 06.5mm) in the treatment of partially or totally edentulous jaws for the purpose of restoring chewing function.

The Straumann® CARES® Screw-retained Bridge Titanium is available in different sizes and spans and can be fitted on 2 to 16 implants.

The Straumann® CARES® Dolder® Bar Titanium is available in different sizes and spans and can be fitted on 2 to 10 implants.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K112280: Straumann Cares Screw-Retained Bridge Titanium, Straumann Cares Dolder Bar Titanium.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K112280

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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