FDA Device Intelligence
Home › SURGIX MEDICAL LLC › FusionMax

FusionMax

SURGIX MEDICAL LLC · Model 33501DC · UDI-DI 10840343716827

KME Prescription
10
510(k) clearances
94
Adverse events
2
Recalls
594
Facilities

Description

Disposable cover kit - Case of 10 - UDI issued by FDA

Recalls

DateFirmReason
2023-06-23Microtek Medical Inc.Certain lots of the products have a Naphthalene odor.
2017-12-27LITTLE RAPIDS CORPORATIONThe secondary supplier provided material was within specification but did not meet our design needs compared to the primary manufacturer. The product is designed for patient trans

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.