22 results · 38ms · Sources: EU EUDAMED, US FDA

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XLTEK EVOKED POTENTIAL HEADBOX, MODEL EP-4-RP (PROPOSED)

FDA 510(k)
FDA Class 2 ·Neurology

Avitene

FDA UDI
Davol Inc.·00801741010460·Avitene Non-Woven Web, 70 mm x 35 mm x 1 mm

PUMA-G System™

FDA UDI
Coaptech, Inc.·10860312001532·External Magnet in Case

Batrik In-Brush Twisted Wire Brushes

FDA UDI
Batrik Medical Manufacturing Inc·00690521005594·Brush\7Fraizier\BD-2.30mm\BL-25.4mm\OL-250mm - ...

Santis Pre Bent Rod 5.5mmx90mm

FDA UDI
Lanterna Medical Technologies GmbH·07640159550648·Santis Pre Bent Rod 5.5mmx90mm

SANTIS™ PRE BENT ROD 5.5mm X90mm -STERILE

FDA UDI
Lanterna Medical Technologies GmbH·07640159551768·SANTIS™ PRE BENT ROD 5.5mm X90mm -STERILE

Integrity-SI Fusion System

FDA UDI
Lincotek Medical LLC·B57112521010090D0·10 x 90 mm Anodized SI Implant

mahe medical GmbH

FDA UDI
mahe medical gmbh·04050659173415·6.5 Cancellous Bone Shaft Screw, hex, _x000D_...

GMA 2.0 Pedicle Screw System

FDA UDI
GRAFTON MEDICAL ALLIANCE, INC.·00810021380292·PRE-BENT ROD, ø5.5 X 90

6.5 Cancellous Bone Shaft Screw, hex, St.Steel, L 90/16 mm

FDA UDI
mahe medical gmbh·EMAH00100100900·6.5 Cancellous Bone Shaft Screw, hex, St.Ste...

METHAFILCON A

FDA 510(k)
FDA Class 2 ·Ophthalmic

GUTHRIE PRIME POWDER-FREE CHLORINATED PATIENT EXAMINATION GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

SEE H10

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code NBC·April 18, 2013

MEDSTONE LITHOTRIPTOR

FDA Adverse Event
Malfunction ·HEALTHTRONICS, INC.·Product code LNS·June 12, 2017

ACIST

FDA Adverse Event
Injury ·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·February 10, 2012

AXSYM DIGOXIN III

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013

ACCU-CHEK ® COMFORT CURVE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·March 8, 2011

ACIST

FDA Adverse Event
Malfunction ·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·April 20, 2007

ACIST

FDA Adverse Event
Injury ·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·February 10, 2012