Home › SYNTHES (U.S.A.) LP › NA

NA

SYNTHES (U.S.A.) LP · Model 389.321 · UDI-DI 10705034775487

HWM Prescription

510(k) clearances

767

Adverse events

Recalls

254

Facilities

Description

DISC RONGEUR-STRAIGHT 4MM WIDTH/400MM LENGTH

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 key Read 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.