510(k) Report

510(k) · Cleared

Cleared

Nobelperfect Conical Connection

K062936510(k) TraditionalCleared Dec 19, 200682-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

Nobel Biocare AB · DZE Implant, Endosseous, Root-Form

Cleared on Dec 19, 2006 as substantially equivalent to K050258 (Nobel Biocare AB, 2005) and 1 other predicate after an 82-day review. Its family tree reaches back 7 generations to 1990. 1 later device descends from it.

Decided
Dec 19, 2006
Review
82 days
Class
Class II
Product code
DZE
Recalls
None
Predicates
2

Its longest line of descent runs back 7 generations to K894595 (1990). 21 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 7 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
  2. 6 generations backK984104 Iti Dental Implant SystemStraumann USA · 1999 · Recalled
  3. 5 generations backK993595 Nobel Biocare's Modified Surface Implant (Intended for Immediate…Nobel Biocare Uas, Inc. · 2000
  4. 4 generations backK023113 Replace Tiunite Endosseous ImplantNobel Biocare Uas, Inc. · 2002 · Recalled
  5. 3 generations backK041661 Nobel Biocare Endosseous ImplantsNobel Biocare Uas, Inc. · 2004
  6. 2 generations backK050258 Groovy ImplantsNobel Biocare AB · 2005 · Recalled
  7. 1 generation backK061003 SFB & CFB ImplantsNobel Biocare AB · 2006
  8. This deviceK062936 Nobelperfect Conical ConnectionNobel Biocare AB · 2006
  9. Descendant · cites it directly · 0 of its ownK072980 Nobelperfect Conical Connection Hexagonal ImplantsNobel Biocare AB · 2007

Most influential descendants

Showing 1 of 1 · See all
  • K072980Nobelperfect Conical Connection Hexagonal ImplantsNobel Biocare AB · 2007 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K894595Bonefit R Screw ImplantsInstitut Straumann AG1990—
−6K984104Iti Dental Implant SystemStraumann USA19991
−5K993595Nobel Biocare's Modified Surface Implant (Intended for Immediate Loading Upon…Nobel Biocare Uas, Inc.2000—
−4K023113Replace Tiunite Endosseous ImplantNobel Biocare Uas, Inc.200227
−3K041661Nobel Biocare Endosseous ImplantsNobel Biocare Uas, Inc.2004—
−2K050258Groovy ImplantsNobel Biocare AB200528
−1K061003SFB & CFB ImplantsNobel Biocare AB2006—
0 (this device)K062936Nobelperfect Conical ConnectionNobel Biocare AB2006—
+1K072980Nobelperfect Conical Connection Hexagonal ImplantsNobel Biocare AB2007—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199320
199420
199630
199720
199810
200230
200510

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200710
FIG. 1 — Lineage of K062936, 1990–2007Source: 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), 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 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? (2)

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
*K050258Groovy Implants
Summary page 1
…(21 CFR 872.3640) Trade or Proprietary or Model Name: NobelPerfect Conical Connection Legally Marketed Device(s): Groovy Implants (K050258) SFB & CFB Implants (K061003) Device Description: Nobel Biocare's NobelPerfect Conical C…
Nobel Biocare AB200528
*K061003SFB & CFB Implants
Summary page 1
…NobelPerfect Conical Connection Legally Marketed Device(s): Groovy Implants (K050258) SFB & CFB Implants (K061003) Device Description: Nobel Biocare's NobelPerfect Conical Connection implants are threaded, root-form dental implants intended f…
Nobel Biocare AB2006—

Also cleared against K050258: 7 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K072980Nobelperfect Conical Connection Hexagonal ImplantsNobel Biocare AB20070

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 16 years and passes through 4 companies; a new generation was cleared every 1.2 years on median.
  • 4 of the 21 ancestors have a recall of any class.
  • Of its descendants, K072980 (Nobel Biocare AB, 2007) has gone furthest, with 0 descendants of its own.
  • 7 other devices also cite its predicate K050258.

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—

What is it indicated for?

Nobel Biocare's NobelPerfect Conical Connection implants are endosseous dental implants intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as an artificial tooth, in order to restore patient esthetics and chewing function. The NobelPerfect Conical Connection implants are indicated for single or multiple unit restorations. The NobelPerfect Conical Connection implants can be used in splinted or non-splinted applications. The NobelPerfect Conical Connection implant may be placed immediately and put into immediate function provided that initial stability requirements detailed in the manual are satisfied.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K062936: Nobelperfect Conical Connection.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K062936

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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