32 results · 23ms · Sources: EU EUDAMED, US FDA

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Collagen Dental Wound Dressings

FDA 510(k)
FDA Unclassified ·Unknown

Column, Sodasorb Disposable, 5.75" L

FDA UDI
A-M SYSTEMS, LLC·00817081026047·Column, Sodasorb Disposable, Prefilled, 5.75" L

CARBON FIBER ROD, Ø9.5mm x 600mm

FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665005455·

Ophthalmic Speculum

FDA UDI
KATENA PRODUCTS, INC.·00841668100431·LANCASTER EYE SPECULUM SOLID

UniTip Catheter

FDA UDI
Unisensor AG·07640172972397·

UniTip Catheter

FDA UDI
Unisensor AG·07640172972403·

DELUXE 18G MICRO CANNULA SET

FDA UDI
The Wells Johnson Company·B458201526000·Cannula Set, Deluxe 18g Micro Cannula Set, cont...

II Ring Retractor

FDA UDI
Automated Medical Products Corp.·00810118341465·Malleable Retractor 4" x 10" with Protective Edge

ZIMMER DENTAL HEX-LOCK PREPARED ABUTMENT (STRAIGHT & ANGLED)

FDA 510(k)
FDA Class 2 ·Dental

SIMPLYGO BREAST PUMP

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

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 10, 2020

EQUINOXE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·March 26, 2021

LIFEPAK(R) 1000 DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·July 10, 2015

DEPUY SYNTHES UNIVERSAL HANDLE

FDA Adverse Event
Injury ·DEPUY SYNTHES·Product code LXH·October 2, 2014

AGILIS NXT, 8.5F, STEERABLE INTRODUCER, MED CURL

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC. (AF-MINNETONKA)·Product code DYB·June 5, 2013

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 27, 2011

CD HORIZON® FENESTRATED SCREW SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·September 3, 2024

LIFEPAK® 1000 DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·April 24, 2019

CD HORIZON® SOLERA¿ FENESTRATED SCREW SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code NKB·July 28, 2025

CD HORIZON® SOLERA¿ FENESTRATED SCREW SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code NKB·July 28, 2025