FDA applicant

Sybron Implant Solutions GmbH

Orange, CA1 decision2009–20090 recalls

FDA records 1 decision for Sybron Implant Solutions GmbH (Orange, CA) in 2009: 1 510(k) clearance. All are in product code DZE (Implant, Endosseous, Root-Form). Its devices cite 1 predicate, 0 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 Sybron Implant Solutions GmbH’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2009high 1 (2009) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Sybron Implant Solutions GmbH by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Sybron Implant Solutions GmbH’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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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/Analytic 3 Sybron Endo 1

Sybron Implant Solutions GmbH

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Sybron”