FDA Device Intelligence
Home › MANI, INC. › MANI ENT Knife

MANI ENT Knife

MANI, INC. · Model NKT35C · UDI-DI 14546951370586

KTG
5
510(k) clearances
15
Adverse events
0
Recalls
97
Facilities

Description

MANI ENT Knife

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.