35 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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GMK FULL PE TIBIAL COMPONENTS
FDA 510(k)
FDA Class 2
·Orthopedic
GMK-PRIMARY FEMUR PS CEMENTED SIZE 6 L
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·July 16, 2020
GMK-PRIMARY FEMUR PS CEMENTED SIZE 4
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·May 22, 2019
GMK-PRIMARY FEMUR PS CEMENTED SIZE 4 LEFT
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·August 23, 2017
GMK-PRIMARY FEMUR PS CEMENTED SIZE 6 L
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·September 25, 2018
Aequalis™ Adjustable Reversed
FDA UDI
TORNIER, INC.·00846832068289·
NC Multi-base Abutment
FDA UDI
BIO CONCEPT Co., Ltd.·06947600306030·
CASTROVIEJO CORNEOSCLERAL SCISSORS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896014190·CASTROVIEJO CORNEOSCLERAL SCISSORS SMALL LEFT A...
Compressyn Staple
FDA UDI
DALLEN MEDICAL, INC.·00850815007080·
Compressyn Staple
FDA UDI
DALLEN MEDICAL, INC.·B470PEZ1313101·
Dukal
FDA UDI
Dukal LLC·00665973002651·Gauze Pad 3" x 3" 12-Ply, Sterile
TAI SHENG VARIOUS NEOX POWERED MUSCLE STIMULATOR
FDA 510(k)
FDA Class 2
·Physical Medicine
VU APOD INTERVERTEBRAL BODY FUSION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523100989·L CR E-MAXTM Vitamin E Congruent Tibial Insert ...
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523165490·L CR Tibial Insert Trial with Anterior Slot, Sz...
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523144471·L CR UHMWPE Congruent Tibial Insert Sz B 10mm
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523101849·L CR MAXTM HXL Congruent Tibial Insert Sz B 10mm
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523124060·L CR Tibial Insert Trial Sz B 10mm
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523172405·CR Tibial Insert Trial with Posterior Pin Relie...
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·March 8, 2021