25 results · 28ms · 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.

ANEURYSM CLIPS

FDA 510(k)
FDA Class 2 ·Neurology

SOLIDEA

FDA UDI
CALZIFICIO PINELLI SRL·08300496013136·RELAX UNISEX 70, SIZE L, ECRU, GRADUATED COMPRE...

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450473962·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033464601·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033464649·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033464618·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033464625·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033464595·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033464632·

CosmoLock Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07310K0131300·Rod Inserter, Articulating, MIS

Flexcera Smile A3

FDA UDI
Envisiontec GmbH·04260683220300·Flexcera Smile is a light-curing material for t...

OCULAR SCIENCES, INC. BIOMEDICS 52 (OCUFILCON D) UV BLOCKING DAILY WEAR SOFT CONTACT LENS

FDA 510(k)
FDA Class 2 ·Ophthalmic

APEX FIXATION PINS

FDA 510(k)
FDA Class 2 ·Orthopedic

IMMULITE 2000 3GALLERGY SPECIFIC IGE

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code DHB·May 22, 2018

IMMULITE 2000 3GALLERGY SPECIFIC IGE

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code DHB·May 22, 2018

CONTACT DETACH

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·November 3, 2025

PFC*SIGMA TC3 FEM RT SZ2

FDA Adverse Event
Injury ·DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDICS·Product code JWH·March 20, 2013

ARCHITECT I2000SR ANALYZER

FDA Adverse Event
Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·March 10, 2011

HVTUNKNOWN

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code LWR·March 12, 2008

UNKNOWN

FDA Adverse Event
Malfunction ·COOK INC·Product code BWC·September 4, 2019