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

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BIOPRO - INFINITY PLATE ANCHOR SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

RC Screw-retained Abutment

FDA UDI
BIO CONCEPT Co., Ltd.·06947600303503·

Endo Carry-On Procedure Kit

FDA UDI
MEDIVATORS INC.·00677964093029·Endo Carry-On Procedure Kit

Endo Carry-On Procedure Kit

FDA UDI
MEDIVATORS INC.·00677964093005·The ENDO CARRY-ON Procedure Kit contains all of...

Aileron Posterior Fusion System

FDA UDI
Life Spine, Inc.·00190837000318·

Aileron Posterior Fusion System

FDA UDI
Life Spine, Inc.·00190837000301·

ACON QUIK-CHECK II MIDSTREAM HOME PREGNANCY TEST

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

DIMENSIONS HB1C KIT, MODEL DF105A

FDA 510(k)
FDA Class 2 ·Hematology

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523144655·L CR UHMWPE Ultracongruent Tibial Insert Sz C 10mm

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523124244·L Ultracongruent Tibial Insert Trial Sz C 10mm

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523164493·L Ultracongruent Tibial Insert Trial with Anter...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102020·L CR MAXTM HXL Ultracongruent Tibial Insert Sz ...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523101160·L CR E-MAXTM Vitamin E Ultracongruent Tibial In...

GUARDIAN¿ SCREW, 5MM, BURR HOLE COVER

FDA Adverse Event
Injury ·ABBOTT MEDICAL·Product code MHY·November 9, 2022

FUJIFILM 600 SERIES ENDOSCOPE EC-600WM

FDA Adverse Event
Malfunction ·FUJIFILM CORPORATION·Product code FDF·January 22, 2025

SWIFT-LOCK ANCHOR

FDA Adverse Event
Injury ·ABBOTT MEDICAL·Product code GZB·October 25, 2022

SWIFT-LOCK ANCHOR

FDA Adverse Event
Injury ·ABBOTT MEDICAL·Product code GZB·October 25, 2022

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 1, 2014

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

PERIFIX

FDA Adverse Event
B. BRAUN MEDICAL ,INC.·Product code CAZ·June 6, 2011