FDA Device Intelligence
Home › TRANZONIC COMPANIES, THE › Maxithins

Maxithins

TRANZONIC COMPANIES, THE · Model MT200 · UDI-DI 00075289047701

HHD
10
510(k) clearances
138
Adverse events
0
Recalls
314
Facilities

Description

MAXITHINS REGULAR MAXI W/WINGS VEND PACK 200/CS

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.