FDA Device Intelligence
HomeFOURSTAR GROUP INC. › B-PURE

B-PURE

FOURSTAR GROUP INC. · Model 24418380 · UDI-DI 00049696508261

LYG
10
510(k) clearances
11
Adverse events
0
Recalls
179
Facilities

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.