FDA applicant

Beverly Hills Prosthetics Orthotics, Inc.

Los Angeles, CA1 decision2002–20020 recalls

FDA records 1 decision for Beverly Hills Prosthetics Orthotics, Inc. (Los Angeles, CA) in 2002: 1 510(k) clearance. All are in product code MVA (Orthosis, Cranial). 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, neurology panel, where it files most

How often FDA has decided Beverly Hills Prosthetics Orthotics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Beverly Hills Prosthetics Orthotics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Beverly Hills Prosthetics Orthotics, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Beverly Hills Prosthetics Orthotics…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Beverly”

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

Beverly Hills Exercise Equipment 1 Beverly Ent., Inc. 1

Beverly Hills Prosthetics Orthotics, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Beverly”