FDA Device Intelligence
Home › Erismet OU › ESTCARBON

ESTCARBON

Erismet OU · Model L992 · UDI-DI 04744946010384

KYS
1
510(k) clearances
32
Adverse events
0
Recalls
124
Facilities

Description

Carbon Fiber Insole, W9/M8-8.5 (9.92 inch)

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.