21 results · 23ms · Sources: EU EUDAMED, US FDA

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HM-CRYO

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

FIXOS

FDA UDI
Stryker GmbH·07613252708797·Lid Screw-Rack 4.0mm

Reef TH

FDA UDI
Seaspine Orthopedics Corporation·10889981203399·Interbody, 9mm x 40mm x 14mm, 0 deg

Reef TA

FDA UDI
Seaspine Orthopedics Corporation·10889981195403·Interbody, 9mm x 40mm x 14mm, 0 deg

Arthrex®

FDA UDI
ARTHREX, INC.·00888867060364·ECLIPSE RESECT PROTECTOR,SZ S/40.0MM

IQ GUIDE WIRE

FDA 510(k)
FDA Class 2 ·Cardiovascular

DOPPLER IMAGING OPTION

FDA 510(k)
FDA Class 2 ·Radiology

UNKNOWN

FDA Adverse Event
WILLIAM COOK EUROPE·Product code DTK·October 27, 2015

ECLIPSE RESECT PROTECTOR,SZ M/46.0MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·May 29, 2024

ECLIPSE RESECT PROTECTOR,SZ L/50.0MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·May 23, 2024

ECLIPSE RESECT PROTECTOR,SZ M/46.0MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·May 23, 2024

ECLIPSE RESECT PROTECTOR,SZ S/40.0MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·June 3, 2024

AVL 6MM SUPERIOR DRILL, MODULAR

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code HWE·May 23, 2024

3.0MM DRILL BIT

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code HTW·June 7, 2024

ECLIPSE RESECT PROTECTOR,SZ S/40.0MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·October 1, 2024

ECLIPSE RESECT PROTECTOR,SZ S/40.0MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·October 1, 2024

ECLIPSE RESECT PROTECTOR,SZ S/40.0MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·October 1, 2024

ECLIPSE RESECT PROTECTOR,SZ S/40.0MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·October 1, 2024

V.A.C. ATS

FDA Adverse Event
Injury ·KCI USA INC.·Product code OMP·June 19, 2014

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 2, 2013