FDA Device Intelligence
Home › VIVE HEALTH LLC › CoreTech

CoreTech

VIVE HEALTH LLC · Model SUP2031BLK · UDI-DI 00810041980458

ISR
1
510(k) clearances
8
Adverse events
0
Recalls
147
Facilities

Description

626 8" Lumbar Back Brace

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.