21 results · 21ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

SOMATOM P30 CT SYSTEMS

FDA 510(k)
FDA Class 2 ·Radiology

ACUFEX

FDA UDI
Smith & Nephew, Inc.·03596010090904·6 MM GRAFT SIZING TUBE

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526189713·LEVAMED ACTIVE ANKLE SUP BLACK L II

Gaudi

FDA UDI
NETBIOLOGICS, LLC·G682G0135221·Fixation Screw, for Gaudi Plate, OD=3.5mm, LEN=...

ASPHERE M SPEC 12/14 36 +1.5

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·September 30, 2024

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033510377·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033510421·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033510384·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033510407·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033510391·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033510445·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033510438·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033510414·

SALUTE

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

SUREVUE URINE HCG

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

BD¿ LUER SLIP SYRINGE STERILE, SINGLE USE, 10 ML

FDA Adverse Event
Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·June 20, 2022

12/14 ARTICUL 40MM M SPEC+5

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·March 20, 2013

ACCESS® 2 IMMUNOASSAY SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER INC.·Product code LTJ·March 10, 2011

MARQUIS DR

FDA Adverse Event
Injury ·MEDTRONIC S.A.·Product code LWS·March 10, 2008

DEK BL MF 0 TC-43/HR 26 2N 36"

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code MFJ·March 14, 2017