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HU-FRIEDY MFG. CO., LLC · Model TNCI5300 · UDI-DI 10889950099541

EIY

510(k) clearances

Adverse events

Recalls

189

Facilities

Description

XTS W3/GFT3 PLASTIC FILLING INSTRUMENT

Query this across every FDA database — by API.

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.