FDA Device Intelligence
Home › Princeton Medical Group, Inc. › PRINCETON

PRINCETON

Princeton Medical Group, Inc. · Model 19131-21 · UDI-DI 00810158210370

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

Description

RETRACTOR US ARMY DOUBLE ENDED PAIR FIG. 1 21X15MM / 40X15MM FIG. 2 25X15MM / 45X15MM 8.25"

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.