FDA applicant

Orthotic & Prosthetic Lab, Inc.

Webster Groves, MO2 decisions2002–20060 recalls

FDA records 2 decisions for Orthotic & Prosthetic Lab, Inc. (Webster Groves, MO) from 2002 to 2006: 2 510(k) clearances. All are in product code MVA (Orthosis, Cranial). Its devices cite 2 predicates, 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 Orthotic & Prosthetic Lab, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Orthotic & Prosthetic Lab, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Orthotic & Prosthetic Lab, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Orthotic & Prosthetic Lab, Inc.’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 “Orthotic”

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

Orthotic Care Services, Llp 1 Orthotic Solutions, Inc. 1

Orthotic & Prosthetic Lab, Inc.

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 “Orthotic”