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Rapid Response

BTNX Inc · Model D14.5-1V · UDI-DI 10722066007751

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1
510(k) clearances
1
Adverse events
0
Recalls
50
Facilities

Description

AMP1000 BAR300 BUP10 BZO300 COC300 MET1000 MDMA500 OPI2000 MTD300 OXY100 PCP25 THC50 PPX300 TCA1000

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.