510(k) Report

510(k) · Cleared

Cleared

Swede-Vent Implant

K950577510(k) TraditionalCleared Jul 11, 1995165-day reviewClass II21 CFR 872.3640

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

Core-Vent Corp. · DZE Implant, Endosseous, Root-Form

Cleared on Jul 11, 1995 after a 165-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 123 later devices descend from it.

Decided
Jul 11, 1995
Review
165 days
Class
Class II
Product code
DZE
Recalls
None
Predicates
0

123 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2006: 1 descendant cleared2015: 5 descendants cleared2010: 2 descendants cleared2013: 3 descendants cleared2014: 3 descendants cleared2022: 12 descendants cleared2007: 1 descendant cleared2012: 1 descendant cleared2011: 3 descendants cleared2018: 3 descendants cleared2017: 1 descendant cleared2024: 16 descendants cleared2019: 6 descendants cleared2026: 12 descendants cleared2016: 2 descendants cleared2021: 8 descendants cleared2025: 23 descendants cleared2023: 16 descendants cleared2020: 5 descendants cleared1995200020052010201520202025
  1. This deviceK950577 Swede-Vent ImplantCore-Vent Corp. · 1995
  2. Descendant · cites it directly · 122 of its ownK061410 Screw-Vent Implant System, SV;Tapered Screw -Vent Implant System…Zimmer Dental, Inc. · 2006 · Recalled
  3. Descendant · 2 generations on · 98 of its ownK072589 Tapered Screw-Vent Implant, 4.1MM, Models: TSV4B8, B10, B11, B13 and…Zimmer Dental, Inc. · 2007 · Recalled
  4. Descendant · 2 generations on · 94 of its ownK101880 Tapered Screw-Vent T Implant, Tapered Screw-Vent P ImplantZimmer Dental, Inc. · 2010 · Recalled
  5. Descendant · 2 generations on · 88 of its ownK112160 Tapered Screw-Vent X ImplantZimmer Dental, Inc. · 2011 · Recalled
  6. Descendant · 3 generations on · 86 of its ownK170588 DESS Dental Smart SolutionsTerrats Medical SL · 2017

Showing 5 of 123 descendants. See all descendants

Descendants cleared per year

2006: 12007: 12010: 22011: 32012: 12013: 32014: 32015: 52016: 22017: 12018: 32019: 62020: 52021: 82022: 122023: 162024: 162025: 232026: 12
2006high 23 (2025) · low 0 (2008)2026

Most influential descendants

Showing 5 of 123 · See all
  • K061410Screw-Vent Implant System, SV;Tapered Screw -Vent Implant System, TSV;Advent Implant…Zimmer Dental, Inc. · 2006 · cites it directly122descendants
  • K072589Tapered Screw-Vent Implant, 4.1MM, Models: TSV4B8, B10, B11, B13 and B16, TSV4H8, H11…Zimmer Dental, Inc. · 2007 · 2 generations on98descendants
  • K101880Tapered Screw-Vent T Implant, Tapered Screw-Vent P ImplantZimmer Dental, Inc. · 2010 · 2 generations on94descendants
  • K112160Tapered Screw-Vent X ImplantZimmer Dental, Inc. · 2011 · 2 generations on88descendants
  • K170588DESS Dental Smart SolutionsTerrats Medical SL · 2017 · 3 generations on86descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K950577Swede-Vent ImplantCore-Vent Corp.1995—
+1K061410Screw-Vent Implant System, SV;Tapered Screw -Vent Implant System, TSV;Advent…Zimmer Dental, Inc.20061
+2K072589Tapered Screw-Vent Implant, 4.1MM, Models: TSV4B8, B10, B11, B13 and B16…Zimmer Dental, Inc.20073
+2K101880Tapered Screw-Vent T Implant, Tapered Screw-Vent P ImplantZimmer Dental, Inc.20101
+2K112160Tapered Screw-Vent X ImplantZimmer Dental, Inc.201119
+3K170588DESS Dental Smart SolutionsTerrats Medical SL2017—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200610
200710
201020
201130
201210
201330
201430
201550
201620
201710
201830
201960
202050
202180
2022120
2023160
2024160
2025230
2026120
FIG. 1 — Lineage of K950577, 1995–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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

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

Planning a device in DZE? 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 DZE device

  1. #1 K211090 ZENEX Implant Systemscore 25.4 · 15 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?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (123)

See all 123

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K061410Screw-Vent Implant System, SV;Tapered Screw -Vent Implant System, TSV;Advent Implant…Zimmer Dental, Inc.2006122

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?

  • Of its descendants, K061410 (Zimmer Dental, Inc., 2006) has gone furthest, with 122 descendants of its own.

How does its category compare?

All DZE devices

DZE Implant, Endosseous, Root-Form: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · DZE

31in 2025

2007: 432008: 612009: 412010: 342011: 262012: 392013: 422014: 362015: 362016: 402017: 482018: 412019: 312020: 412021: 342022: 342023: 352024: 402025: 312026 (partial year): 15
2007high 61 (2008) · low 26 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DZE

184in 2025

2007: 107 days median2008: 118 days median2009: 110 days median2010: 162 days median2011: 194 days median2012: 174 days median2013: 195 days median2014: 265 days median2015: 215 days median2016: 219 days median2017: 223 days median2018: 200 days median2019: 231 days median2020: 230 days median2021: 182 days median2022: 243 days median2023: 248 days median2024: 222 days median2025: 184 days median2026 (partial year): 194 days median
2007high 265 (2014) · low 107 (2007)2026

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

Recalls per year · DZE

1in 2025

2007: 112008: 42009: 32010: 32012: 112013: 12014: 72015: 32016: 152017: 42018: 42019: 82021: 62024: 12025: 12026 (partial year): 2
2007high 15 (2016) · low 0 (2011)2026

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

Adverse event reports per year · DZE

465,788in 2025

2007: 2252008: 3932009: 1642010: 3602011: 3622012: 3582013: 3912014: 1,1242015: 2,8942016: 1,1162017: 9,7192018: 12,8922019: 167,0162020: 255,5242021: 479,6182022: 483,2242023: 537,5852024: 473,6292025: 465,788
2007high 537,585 (2023) · low 164 (2009)2025

MAUDE reports naming product code DZE, 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
20074310711225
2008611184393
2009411103164
2010341623360
2011261940362
20123917411358
2013421951391
20143626571,124
20153621532,894
201640219151,116
20174822349,719
201841200412,892
2019312318167,016
2020412300255,524
2021341826479,618
2022342430483,224
2023352480537,585
2024402221473,629
2025311841465,788
2026151942—

More from Core-Vent Corp.

25 FDA decisions under this applicant name. See the company

  • K002614Advent Implant SystemCore-Vent Corp. · 2000
  • K002188Swissplus Implant System, Model SPWB 8,10,12,14/OPH20/SMPR, SPB 8,10,12,14/OP3.5D/Opar,Opb…Core-Vent Corp. · 2000
  • K950576Bio-Vent X ImplantCore-Vent Corp. · 1995
  • K950575Bio-Vent ImplantCore-Vent Corp. · 1995
  • K950578Screw-Vent ImplantCore-Vent Corp. · 1995

Recent decisions in DZE

The DZE category page

  • K261295MultiNeO Dental Implant SystemAlpha Bio Tec, Ltd. · 2026
  • K261392TriActive Dental Implant SystemParagon Implant Mfg., LLC · 2026
  • K260463ZEROS Dental Implant SystemZeros Co., Ltd. · 2026
  • K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd. · 2026
  • K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd. · 2026

https://510kreport.com/device/K950577 · printed Nov 4, 2026

Cite this page

510(k) Report. “K950577: Swede-Vent Implant.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K950577

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026