FDA Device Intelligence
Home › Conmed Corporation › FLX-LITE

FLX-LITE

Conmed Corporation · Model 3058A · UDI-DI 10845854044353

KYT Prescription
6
510(k) clearances
10
Adverse events
1
Recalls
159
Facilities

Description

FLX-LITE, FLEXIBLE SURGICAL LITE, 127 MM (5")

Recalls

DateFirmReason
2023-03-20DermLite LLCIncorrect labeling; Package labeling contains a different serial number then the serial number on the product labeling.

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.