141 results · 29ms · Sources: EU EUDAMED, US FDA

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FLARE Single-Use Surgical Laser Fiber

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

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112571·BARRON CORNEAL PUNCH 6.5MM

OsteoMed

FDA UDI
OSTEOMED LLC·00845694041553·Plate File

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112717·BARRON VACUUM PUNCH 6.5MM

PURE PECTUS

FDA UDI
KLS-Martin L.P.·00888118147073·LID, STABILIZERS

NEUROTOLOGY DRAPE, MODEL TBD

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

POWDERED SYNTHETIC VINYL EXAM GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

BALL HEADS: MECTACER BIOLOX DELTA CERAMIC BALL HEAD 12/14 Ø 32 SIZE L

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·July 16, 2024

CLEARLINK/DUO-VENT

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·January 30, 2026

GMK PRIMARY TOTAL KNEE SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·March 3, 2026

GMK-SPHERE TIBIAL INSERT FIXED SPHERE CR SIZE 4/10 MM R

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 28, 2023

HIGH V+ Spinal Cement System REF T040321K

FDA Recall
Open, Classified ·TEKNIMED SAS Zone Industrielle Montredone 11 Rue D Apollo L'Union France·Product code NDN·December 15, 2022

CUP: MPACT DOUBLE MOBILITY ACETABULAR SHELL Ø56

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·July 7, 2023

COAGUCHEK XS PT TEST PST

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·May 7, 2026

GMK-SPHERE 02.07.1205R TIBIAL TRAY FIXED CEMENTED SIZE 5 R

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·March 30, 2023

GMK-SPHERE PATELLA RESURFACING SIZE 3

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 1, 2024

EON MINI

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·October 22, 2014

CELL-DYN RUBY ANALYZER

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·August 11, 2011

SYNCHROMED II

FDA Adverse Event
Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 2, 2013

GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 4/12 MM L E-CROSS

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·June 5, 2024