10,000 results · 34ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

Techno-Aide

FDA UDI
Techno-Aide, Inc.·G242CPADPPF9·PREMIUM PLUS FIRM TABLE PAD

ITE PRESCRIPTION SERIES MODEL PP + F

FDA 510(k)
FDA Class 1 ·Ear, Nose, Throat

PREFIX PPF

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC·Product code FEC·May 1, 2008

BLOSSOM

FDA UDI
Mexpo International Inc.·00723860977151·POLYCHLOROPRENE EXAMINATION GLOVES POWDER FREE ...

BLOSSOM

FDA UDI
Mexpo International Inc.·00723860977175·POLYCHLOROPRENE EXAMINATION GLOVES POWDER FREE ...

BLOSSOM

FDA UDI
Mexpo International Inc.·00723860977168·POLYCHLOROPRENE EXAMINATION GLOVES POWDER FREE ...

BLOSSOM

FDA UDI
Mexpo International Inc.·00723860977182·POLYCHLOROPRENE EXAMINATION GLOVES POWDER FREE ...

BLOSSOM

FDA UDI
Mexpo International Inc.·00723860977199·POLYCHLOROPRENE EXAMINATION GLOVES POWDER FREE ...

PPF LTZ STEM SZ 07X165MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·April 1, 2026

UNKNOWN PPF-05 STEM HIP IMPL WIN GEN

FDA Adverse Event
Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code KWA·October 20, 2022

UNK HIP FEMORAL STEM CORAIL

FDA Adverse Event
Malfunction ·DEPUY IRELAND - 9616671·Product code LZO·July 19, 2022

UNK - CAGE/SPACERS: SYNCAGE

FDA Adverse Event
Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code OVD·September 19, 2019

466FXXXX

FDA Adverse Event
Injury ·CORDIS CASHEL·Product code DTK·January 4, 2018

ALTRX +4 NEUT 32IDX50OD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 21, 2018

S-ROM M HEAD 36MM +3

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·September 11, 2013

PINN CAN BONE SCREW 6.5MMX30MM

FDA Adverse Event
Injury ·DEPUY RAYNHAM, A DIV. OF DEPUY ORTHO 1219655·Product code LPH·November 1, 2018

STRATTICE RECONSTRUCTIVE TISSUE MATRIX, 10 X 16, FIRM

FDA Adverse Event
Injury ·LIFECELL·Product code FTM·September 5, 2023

UNKNOWN HIP IMPLANT

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·January 3, 2019

SROM STM ST,36+6L NK,11X16X150

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LPH·January 3, 2019

ARTICULEZE M HEAD 36MM +5

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·June 8, 2018