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