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AIR-FLOW

E.M.S. Electro Medical Systems S.A. · Model FT-230W/A · UDI-DI 07613353161965

KOJ Prescription
1
510(k) clearances
19
Adverse events
1
Recalls
24
Facilities

Description

AIRFLOW One basic

Recalls

DateFirmReason
2010-12-13Groman Inc.Groman Inc. of Margate, FL recalled their product Cordless Etcher Air Brush. When non-conforming cartridges are inserted into the Cordless Etcher they can induce excessive stresses

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.