FDA Device Intelligence
Home › SYNTHES (U.S.A.) LP › NA

NA

SYNTHES (U.S.A.) LP · Model PDL324 · UDI-DI 10705034700533

EML Prescription
2
510(k) clearances
45
Adverse events
0
Recalls
160
Facilities

Description

CHISEL 12MM

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.