21 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STARLIGHT
FDA 510(k)
FDA Class 2
·Neurology
N/A
FDA UDI
MEDTRONIC XOMED, INC.·00763000035211·PROSTHESIS 1133250 LIPPY CUP PSTN .6X4.0
Lippy
FDA UDI
MEDTRONIC XOMED, INC.·00681490034609·PROSTHESIS 1133250 LIPPY CUP PSTN .6X4.0
Starbond CoS
FDA UDI
S & S Scheftner GmbH·04260207850358·Ingots, 250g
Oticon
FDA UDI
Oticon A/S·05707131260154·RIA, BTE 13 WL 85 TC
Clear Readers
FDA UDI
Diversified Products, Inc.·00037741113362·
INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR
FDA Adverse Event
Injury
·MSD DEGGENDORF MFG·Product code OVD·December 18, 2019
ADDplus
FDA UDI
Ulrich GmbH & Co. KG·04052536007301·Insert for screwdriver, for screw Ø 5.0 mm
CLYDESDALE PTC SPINAL SYSTEM
FDA Adverse Event
Injury
·MSD DEGGENDORF MFG·Product code MAX·October 17, 2019
CPS DIRECT SL II SLITTABLE OUTER CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
EDWARDS LIFESCIENCES VANTEX CENTRAL VENOUS CATHETERS WITH THERMISTOR
FDA 510(k)
FDA Class 2
·General Hospital
3 ML SYRINGE
FDA Adverse Event
Malfunction
·UNK·Product code FMI·October 14, 2025
DISPENSING PIN
FDA Adverse Event
Malfunction
·UNK·Product code KYX·October 14, 2025
CHARGING SYSTEM
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 20, 2013
L9000 LIGHTSOURCE
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY SAN JOSE·Product code FCW·May 10, 2011
ONE TOUCH ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·August 21, 2008
M2A-MAGNUM MOD HD SZ 44MM 44MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·June 3, 2024
MALLORY HEAD POR FMRL 13X170MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·June 3, 2024
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code NKB·April 19, 2019
M2A-MAGNUM PF CUP 50ODX44ID
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·June 3, 2024