Rapid Response
BTNX Inc · Model D9.17-1VF · UDI-DI 10722066008093
1
510(k) clearances
1
Adverse events
0
Recalls
60
Facilities
Description
D9.17-1VF- COC300 OPI2000 AMP1000 MET1000 BAR300 BZO300 MDMA500 MTD300 PCP25
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.
