FDA Device Intelligence
Home › SONTEC INSTRUMENTS, INC. › LUER RETRACTOR

LUER RETRACTOR

SONTEC INSTRUMENTS, INC. · Model 502-405 · UDI-DI 00192896089624

KAL Prescription
5
510(k) clearances
15
Adverse events
1
Recalls
124
Facilities

Description

LUER RETRACTOR DOUBLE ENDED S-SHAPED TIPS

Recalls

DateFirmReason
2023-05-25TELEFLEX LLCThere are incomplete pre-cleaning instructions within the Instructions for Use (IFU).

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.