PROCARE
DJO, LLC · Model 79-95515-0136 · UDI-DI 00190446135401
7
510(k) clearances
121
Adverse events
0
Recalls
210
Facilities
Description
XCELTRAX, AIR, MEDIUM, CDA FOOT AND ANKLE
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 docsData 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.