FDA applicant

Sybron Endo/Analytic

Orange, CA3 decisions2002–20043 recalls

FDA records 3 decisions for Sybron Endo/Analytic (Orange, CA) from 2002 to 2004: 3 510(k) clearances. Most are in product codes ELC (Scaler, Ultrasonic) and EAT (Tester, Pulp). 3 recalls are 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 Sybron Endo/Analytic’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sybron Endo/Analytic since 2007.

Recalls per year

1in 2017

2007high 2 (2013) · low 0 (2007)2026

Class I Class II/III not classified

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

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Other applicant names beginning “Sybron”

FDA records each applicant name separately; these may or may not be the same firm.

Sybron Dental Specialties, Inc. 121 Sybron Corp. 37 Sybron Endo 1 Sybron Implant Solutions GmbH 1

Sybron Endo/Analytic

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Sybron”