FDA applicant

Angstrom Mfg., Inc.

Bloomsdale, MO2 decisions2011–20110 recalls

FDA records 2 decisions for Angstrom Mfg., Inc. (Bloomsdale, MO) in 2011: 2 510(k) clearances. All are in product code EGS (Handpiece, Contra- And Right-Angle Attachment…). 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 Angstrom Mfg., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2011

2011high 2 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Angstrom Mfg., Inc. by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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See the 510(k) Report

Other applicant names beginning “Angstrom”

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

Angstrom Medica, Inc. 1

Angstrom Mfg., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Angstrom”