FDA Device Intelligence
Home › TRI-ANIM HEALTH SERVICES, INC. › Curaplex

Curaplex

TRI-ANIM HEALTH SERVICES, INC. · Model 301-6000T · UDI-DI 00818834021029

BYX
10
510(k) clearances
518
Adverse events (14 deaths)
1
Recalls
232
Facilities

Description

**TEE PIECE 50/BG

Recalls

DateFirmReason
2018-08-10A M Systems IncSome of the Disposable Smooth Interior Tubing may pull apart when stretched.

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.