FDA applicant

Safe Bvm Corporation

Chesterfield, MO1 decision2022–20220 recalls

FDA records 1 decision for Safe Bvm Corporation (Chesterfield, MO) in 2022: 1 510(k) clearance. All are in product code BTM (Ventilator, Emergency, Manual (Resuscitator)). 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, anesthesiology panel, where it files most

How often FDA has decided Safe Bvm Corporation’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2022high 1 (2022) · low 0 (2023)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2022.

FIG. 1 — Safe Bvm Corporation by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Safe Bvm Corporation’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 “Safe”

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

Safe Orthopaedics 13 Safe Shield Co., Ltd. 2 Safe Tech Medical Products, Inc. 2 Safe-Tec Clinical Products, Inc. 2 Safe Secure Packaging Co., Ltd. 2 Safe Glove, Ltd. 2 Safe Obstetric Systems, Ltd. 1 Safe Product Supplies 1 Safe T Medical Devices, Ltd. 1 Safe Secure Packing Co., Ltd. 1 Safe Restraints, Inc. 1 Safe Sun Corporation of America, Inc. 1

Safe Bvm Corporation

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Safe”