FDA Device Intelligence
Home › Supracor, Inc. › Supracor Stimulite Honeycomb

Supracor Stimulite Honeycomb

Supracor, Inc. · Model PDCD1313 · UDI-DI 00842749106977

IMP
2
510(k) clearances
134
Adverse events (1 deaths)
1
Recalls
171
Facilities

Recalls

DateFirmReason
2014-01-31Bock,Otto,Orthopedic Ind,IncOtto Bock is recalling all Aerial and Aerial Active Wheelchair Cushions from specific material numbers. During internal testing, it was discovered that there is a small risk of fl

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.