510(k) Report

FDA applicant

Est. Anthogyr

Sallanches, FR3 decisions2002–20070 recalls

FDA records 3 decisions for Est. Anthogyr (Sallanches, FR) from 2002 to 2007: 3 510(k) clearances. Most are in product codes EFA (Handpiece, Belt And/Or Gear Driven, Dental) and EGS (Handpiece, Contra- And Right-Angle Attachment…). Its devices cite 8 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

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

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Est. Anthogyr’s devices, and how often a recall has named them.

FDA decisions per year

1in 2007

2007: 1
2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Est. Anthogyr by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • EFAHandpiece, Belt And/Or Gear Driven, Dental1decision
  • EGSHandpiece, Contra- And Right-Angle Attachment, Dental1decision
  • ELRPost, Root Canal1decision

Whose devices does it build on?

Its devices cite 8 predicates; 1 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 4 times; 1 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K060317Anthogyr Contra Angles and HandpiecesEst. Anthogyr · 20062cite it
  • K070084Montblanc Implantology Contra Angle ControlEst. Anthogyr · 20071cites it
  • K020431FibiocoreEst. Anthogyr · 20021cites it

What has FDA decided for it lately?

  • K070084Montblanc Implantology Contra Angle ControlEst. Anthogyr · 2007
  • K060317Anthogyr Contra Angles and HandpiecesEst. Anthogyr · 2006
  • K020431FibiocoreEst. Anthogyr · 2002

All 3 as Est. Anthogyr →