41 results · 21ms · Sources: EU EUDAMED, US FDA

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Nihon Kohden CSM 1901 Bedside Monitor

FDA 510(k)
FDA Class 2 ·Cardiovascular

LIFE SCOPE G9

FDA Adverse Event
Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·June 13, 2024

LIFE SCOPE G9

FDA Adverse Event
Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·October 27, 2023

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·24026704282924·ISRAEL RETRACTOR 9 1/2" 4 PRONGS

AGC TRADITION KNEE SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304240964·

STRYKER

FDA UDI
MAKO SURGICAL CORP.·00848486029647·LID, STANDARD

AGXO

FDA UDI
Oticon A/S·05707131284402·H110V2 TI, BTE 13 WL 85 DBL AGXO

BLT Drill, long

FDA UDI
BIO CONCEPT Co., Ltd.·06947600304081·

Ophthalmic Speculum

FDA UDI
KATENA PRODUCTS, INC.·00841668100257·CHU ASPIRATING SPECULUM SOLID

Malibu™

FDA UDI
Seaspine Orthopedics Corporation·10889981030094·PRECONTOURED ESS ROD, 5.5 x 80 mm

Precontoured Rod Ø5.5 mm x80 mm Package

FDA UDI
XENCO MEDICAL LLC·B064XM21510801·

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575292530·Knee femur prosthesis trial - General Instrument

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575292363·Knee femur prosthesis trial - General Instrument

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575292240·Knee femur prosthesis trial - General Instrument

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575292868·Knee femur prosthesis trial - General Instrument

NON STICK BIPOLAR FORCEPS MODEL 07/XXX, BIPOLAR FORCEPS MODEL 08/XXX, MONOPOLAR FORCEPS MODEL 09/XXX

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

PHYSIOLASER OLYMPIC, SINGLE PROBES CW, CLUSTER PROBES CW, LIGHT NEEDLE, PHOTONIC SATELLITE

FDA 510(k)
FDA Class 2 ·Physical Medicine

Ø5.5mm X 80mm PRECONTOURED RODS

FDA UDI
XENCO MEDICAL LLC·B064XMPH21510802·

TriVerse Femoral Trial

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215098469·

BD VACUTAINER® ECLIPSE¿ SIGNAL¿ BLOOD COLLECTION NEEDLE WITH INTEGRATED HOLDER

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·April 24, 2024