FDA Device Intelligence
Home › G & H Wire Company, Inc. › NA

NA

G & H Wire Company, Inc. · Model PWX537 · UDI-DI 10190886154175

EGD Prescription
10
510(k) clearances
8
Adverse events
0
Recalls
201
Facilities

Description

PAT. WAX PACKS, UNSC, 50 PCS

Query this across every FDA database — by API.

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

Get your free API keyRead the docs
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.