161 results · 27ms · Sources: EU EUDAMED, US FDA

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REVLOK FENESTRATED SCREW SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

CoRoent

FDA UDI
Nuvasive, Inc.·00887517563934·CoRoent Ant TLIF PEEK, 11x10x28mm 0°

Medtronic Reusable Instruments

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00721902096075·GUIDE 9110280 TREPHINE TPRD 14MM

DD tempMED

FDA UDI
Dental Direkt GmbH·EDDIK110201·DD tempMED are pre-colored dental milling blank...

TC-100

FDA UDI
Smith & Nephew, Inc.·03596010034663·4-WAY COMBINATION SCREWDRIVER

NIDO Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07315K1102000·Tray, 2 inch base

Marina Medical

FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306815799·Israel Retractor, 4 Prong, 23cm

Apex

FDA UDI
ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529587000·Apex Femoral Nail GT Right Ø 11.0 x 280mm

MAYO LEXER SCISSORS

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896098244·MAYO LEXER SCISSORS ROUND BLADE STRAIGHT TIP

Apex

FDA UDI
ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529588007·Apex Femoral Nail Retrograde Ø 11.0 x 280mm

Apex

FDA UDI
ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529581145·Apex Femoral Nail PF Left Ø 11.0 x 280mm

Apex

FDA UDI
ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529585204·Apex Femoral Nail PF Right Ø 11.0 x 280mm

Apex

FDA UDI
ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529586102·Apex Femoral Nail GT Left Ø 11.0 x 280mm

GYNCARE MORCELLEX TISSUE MORCELLATOR

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

MIDWESTERN REPROCESSING CENTER REPROCESSED PULSE OXIMETER PROBE

FDA 510(k)
FDA Class 2 ·Cardiovascular

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197029957·Metzenbaum-Nelson scissors straig...

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 13, 2013

PUMP IN STYLE ADVANCED BREAST PUMP GO TOTE

FDA Adverse Event
Malfunction ·MEDELA, INC.·Product code HGX·September 10, 2014

ACCU-CHEK RAPID-D LINK

FDA Adverse Event
Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code FPA·May 20, 2011

CAPIOX FX OXYGENATOR

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·October 15, 2024