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

RETRACTOR

KLS-Martin L.P. · Model 48-103-80-07 · UDI-DI 00888118070487

EIG Prescription
8
510(k) clearances
34
Adverse events
0
Recalls
337
Facilities

Description

SOFT TISSUE, OBWEGESER, CURVED DOWN, 16 X 80 MM BLADE

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.