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

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Powder Free White Sterilized Polyisoprene Surgical Gloves-Tested for Use with The Chemotherapy Drugs

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

PLIF Cage

FDA UDI
Eisertech, LLC·B5231003576200915·Lordotic TPLIF Cage, Titanium 20AP X 09ML X 15H...

METZENBAUM SCISSORS

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896055933·METZENBAUM SCISSORS WITH GOLD SCREW CURVED BLAD...

A-CIFT® SoloFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361021476·A-CIFT SoloFuse 4.5 Screw, Lag, 15mm

PLIF Cage

FDA UDI
Eisertech, LLC·B523100097200915·PLIF CAGE, LORDOTIC, 20AP X 09ML X 15HT

SOPRO LIGHT SOURCES AND ACCESSORIES

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

PASTEUR PIPET - STERILE 9, PASTEUR PIPET - STERILE 5 3/4, MODELS 16-PP-9, 16-PP-5.75

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

PLIF Cage

FDA UDI
Eisertech, LLC·B52310035712200915·Lordotic TPLIF Cage, Titanium 20AP X 09ML X 15H...

PLIF Cage

FDA UDI
Eisertech, LLC·B52310035718200915·Lordotic TPLIF Cage, Titanium 20AP X 09ML X 15H...

200915-STAMP PLATFORM/115V

FDA Adverse Event
Injury ·0700-C.R.BARD ELECTROPHYSIOLOGY PRODUCT·Product code DRQ·August 22, 2003

Single Action Biopsy Device

FDA UDI
ARGON MEDICAL DEVICES, INC.·00886333219353·Single Action Biopsy Device 20g (0.9mm) x 9cm

Coaxial SABD Biopsy Device

FDA UDI
ARGON MEDICAL DEVICES, INC.·00886333218387·Coaxial SABD Biopsy Device

VANISH POINT TUBERCULIN SYRINGE

FDA Adverse Event
Malfunction ·RETRACTABLE TECHNOLOGIES, INC.·Product code MEG·March 30, 2021

AZURION

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·April 3, 2026

AZURION

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·January 12, 2026

AZURION

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·April 8, 2026

AZURION

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·July 16, 2025

AZURION

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·March 30, 2026

AZURION

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·May 11, 2026

AZURION

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·May 8, 2026