30 results · 22ms · 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.

Pelvital System

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

OsteoMed

FDA UDI
OSTEOMED LLC·00845694032704·FPS .213 x 9" Partially Threaded Steinman Pin

GUMS SCISSORS

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896054998·GUMS SCISSORS SHARP CURVED BLADES POWER CUT BLACK

Pin

FDA UDI
Treace Medical Concepts, Inc.·00810111224789·Pin

NA

FDA UDI
Biedermann Motech GmbH & Co. KG·04255772609432·MOSS VRS/MIS Locking Instrument HP

OsteoMed

FDA UDI
OSTEOMED LLC·00845694073080·FPS .213 x 9" Partially Threaded Steinman Pin S...

30MM INTRAFIX TIBIAL SHEATH

FDA Adverse Event
Injury ·DEPUY MITEK·Product code MBI·October 15, 2004

8-10MMX 30MM INTRAFIX TAPERED

FDA Adverse Event
Injury ·DEPUY MITEK·Product code MBI·October 15, 2004

MODIFICATION TO T-REX BIOPSY FORCEPS

FDA 510(k)
FDA Class 2 ·Cardiovascular

STEAMPLUS STERILIZATION TEST

FDA 510(k)
FDA Class 2 ·General Hospital

MEDPOR IMPLANT

FDA Adverse Event
Injury ·POREX SURGICAL·Product code JAZ·January 19, 2007

INTERSTIM

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·December 1, 2017

SYNCHROMED II

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·April 18, 2014

COLLEAGUE VOLUMETRIC INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 20, 2008

PRECISION XTRA

FDA Adverse Event
Malfunction ·Product code NBW·August 11, 2011

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

FDA Adverse Event
Malfunction ·INVACARE SUZHOU·Product code CAW·July 1, 2013

TOWEL OR 17X24IN BLUE 2PK X-RAY DETECTAB

FDA Adverse Event
Malfunction ·JIANERKANG MEDICAL DRESSING CO. LTD·Product code FRL·November 18, 2020

TOWEL OR 17X24IN BLUE STERILE 1/PK

FDA Adverse Event
Malfunction ·JIANGSU PROVINCE JIANERKANG MEDICAL·Product code FRL·September 18, 2020

SCREWDRIVER BLADE FOR FRACTURE SCREWS 2.0 / 2.3 / 2.7MM UNIVERSAL FRACTURE MODUL

FDA Adverse Event
Malfunction ·STRYKER LEIBINGER FREIBURG·Product code LXH·April 25, 2014

NEEDLE 25GA 5/8IN

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·December 7, 2020