FDA Device Intelligence
Home › KLS-Martin L.P. › RETRACTOR

RETRACTOR

KLS-Martin L.P. · Model 38-843-19-07 · UDI-DI 00888118064202

EIG Prescription
8
510(k) clearances
34
Adverse events
0
Recalls
336
Facilities

Description

CORONOID, HARGIS, 1 X 2 TEETH, W/CHAIN

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.