FDA applicant

Bryan Keropian Dds

Tarzana, CA4 decisions2005–20090 recalls

FDA records 4 decisions for Bryan Keropian Dds (Tarzana, CA) from 2005 to 2009: 4 510(k) clearances. All are in product code LQZ (Device, Jaw Repositioning). Its devices cite 17 predicates, 5 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 Bryan Keropian Dds’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2007high 1 (2009) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Bryan Keropian Dds’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 “Bryan”

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

Bryan Corp. 5 Bryan Medical, Inc. 4

Bryan Keropian Dds

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 “Bryan”