510(k) Report

510(k) · Cleared

Cleared

Branemark System Drills and Countersinks

K925770510(k) TraditionalCleared Sep 16, 1993304-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

Nobelpharma USA, Inc. · DZE Implant, Endosseous, Root-Form

Cleared on Sep 16, 1993 after a 304-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 574 later devices descend from it.

Decided
Sep 16, 1993
Review
304 days
Class
Class II
Product code
DZE
Recalls
None
Predicates
0

574 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 1997: 3 descendants cleared1996: 1 descendant cleared2005: 5 descendants cleared2007: 9 descendants cleared2008: 9 descendants cleared2004: 7 descendants cleared2010: 10 descendants cleared2006: 8 descendants cleared2017: 27 descendants cleared2015: 28 descendants cleared2016: 35 descendants cleared2018: 28 descendants cleared1998: 1 descendant cleared2013: 16 descendants cleared2009: 14 descendants cleared2012: 14 descendants cleared2019: 27 descendants cleared2020: 43 descendants cleared2011: 15 descendants cleared2024: 60 descendants cleared2026: 26 descendants cleared2022: 37 descendants cleared2025: 44 descendants cleared2021: 40 descendants cleared2023: 46 descendants cleared2014: 21 descendants cleared1990200020102020
  1. This deviceK925770 Branemark System Drills and CountersinksNobelpharma USA, Inc. · 1993
  2. Descendant · cites it directly · 549 of its ownK962403 Noblepharma Wide AccessoriesNobelpharma USA, Inc. · 1996
  3. Descendant · 2 generations on · 545 of its ownK971706 Tiadapt Abutment SystemNobel Biocare Uas, Inc. · 1997
  4. Descendant · 3 generations on · 543 of its ownK974150 Procera Preparable Abutment SystemNobel Biocare Uas, Inc. · 1998 · Recalled
  5. Descendant · 4 generations on · 476 of its ownK032263 3I Patient-Specific Dental Abutment and Overdenture BarImplant Innovations, Inc. · 2004 · Recalled
  6. Descendant · 4 generations on · 441 of its ownK042658 Procera Abutment Branemark, Models 10-4001, 10-4004, 10-5001…Nobel Biocare Uas, Inc. · 2004

Showing 5 of 574 descendants. See all descendants

Descendants cleared per year

1996: 11997: 31998: 12004: 72005: 52006: 82007: 92008: 92009: 142010: 102011: 152012: 142013: 162014: 212015: 282016: 352017: 272018: 282019: 272020: 432021: 402022: 372023: 462024: 602025: 442026: 26
1996high 60 (2024) · low 0 (1999)2026

Most influential descendants

Showing 5 of 574 · See all
  • K962403Noblepharma Wide AccessoriesNobelpharma USA, Inc. · 1996 · cites it directly549descendants
  • K971706Tiadapt Abutment SystemNobel Biocare Uas, Inc. · 1997 · 2 generations on545descendants
  • K974150Procera Preparable Abutment SystemNobel Biocare Uas, Inc. · 1998 · 3 generations on543descendants
  • K0322633I Patient-Specific Dental Abutment and Overdenture BarImplant Innovations, Inc. · 2004 · 4 generations on476descendants
  • K042658Procera Abutment Branemark, Models 10-4001, 10-4004, 10-5001, 10-5004, 10-6001, 10-6004Nobel Biocare Uas, Inc. · 2004 · 4 generations on441descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K925770Branemark System Drills and CountersinksNobelpharma USA, Inc.1993—
+1K962403Noblepharma Wide AccessoriesNobelpharma USA, Inc.1996—
+2K971706Tiadapt Abutment SystemNobel Biocare Uas, Inc.1997—
+3K974150Procera Preparable Abutment SystemNobel Biocare Uas, Inc.19982
+4K0322633I Patient-Specific Dental Abutment and Overdenture BarImplant Innovations, Inc.20041
+4K042658Procera Abutment Branemark, Models 10-4001, 10-4004, 10-5001, 10-5004…Nobel Biocare Uas, Inc.2004—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199610
199730
199810
200470
200550
200680
200790
200890
2009140
2010100
2011150
2012140
2013160
2014210
2015280
2016350
2017270
2018280
2019270
2020430
2021400
2022370
2023460
2024600
2025440
2026260
FIG. 1 — Lineage of K925770, 1993–2026Source: 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 has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (574)

See all 574

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

NumberDeviceApplicantDecidedDescendants
K962403Noblepharma Wide AccessoriesNobelpharma USA, Inc.1996549
K970499Branemark System Zygomaticus Fixture SystemNobel Biocare Uas, Inc.199750

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, K962403 (Nobelpharma USA, Inc., 1996) has gone furthest, with 549 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 Nobelpharma USA, Inc.

64 FDA decisions under this applicant name. See the company

  • K984162Branemark Bone-Anchored Hearing Aid (Baha) System for Pediatric UseNobelpharma USA, Inc. · 1999
  • K962403Noblepharma Wide AccessoriesNobelpharma USA, Inc. · 1996
  • K955713Nobelpharma Bone Anchored Hearing AidNobelpharma USA, Inc. · 1996
  • K962130Branemark Systems Mkii Selk-Tapping FixtureNobelpharma USA, Inc. · 1996
  • K96173617 Angulated AbutmentNobelpharma USA, Inc. · 1996

Recent decisions in DZE

The DZE category page

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  • 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/K925770 · printed Nov 6, 2026

Cite this page

510(k) Report. “K925770: Branemark System Drills and Countersinks.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K925770

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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