35 results · 23ms · 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.

Gx-IVF, Gx-TL, Gx-MOPS PLUS

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

NA

FDA UDI
DEPUY SPINE, LLC·10705034000657·SPINAL INSTRUMENT RONGEUR LIGHT UPPER CURVE 8mm

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112557·BARRON VACUUM TREPHINE 9.0MM

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112977·CORNEAL TREPHINE BLADE9.0MM

THORLAKSON ABDOMINAL HAND RETRACTOR

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896019812·THORLAKSON ABDOMINAL HAND RETRACTOR WITH LIGHT ...

TRANSCURE, MODEL 2910

FDA 510(k)
FDA Class 2 ·Dental

PRONEB ULTRA MODEL NUMBER 85B0100

FDA 510(k)
FDA Class 2 ·Anesthesiology

BD VENFLON¿ PRO SAFETY PERIPHERAL SAFETY IV CATHETER

FDA Adverse Event
Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·November 17, 2021

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·July 30, 2025

23 G X 1 IN. BD INTEGRA¿ 3 ML SYRINGE WITH DETACHABLE NEEDLE

FDA Adverse Event
Injury ·BECTON DICKINSON MEDICAL SYSTEMS·Product code MEG·May 2, 2017

KERAMOS CERAMIC-ON-CERAMIC LINER

FDA Adverse Event
Other ·ENCORE MEDICAL, L.P.·Product code KWB·October 17, 2008

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·August 11, 2011

TOTAL ASR ACET IMP SIZE 60

FDA Adverse Event
Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 2, 2013

Barron Radial Vacuum Trephine (1) Complete Trephine Set 9.0mm Dia. Ref. K20-2062 Lot 122336 Opthalmic

FDA Enforcement
Class II ·Terminated·Surgical Instrument Service And Savings, Inc.·July 10, 2013

Barron Radial Vacuum Trephine (1) Complete Trephine Set 9.0mm Dia. Ref. K20-2062 Lot 122336 Opthalmic

FDA Recall
Terminated ·Surgical Instrument Service And Savings, Inc.·Product code HRH·May 3, 2013

HIP END EFFECTOR, VARIABLE ANGLE

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code OLO·August 31, 2017

HIP END EFFECTOR, VARIABLE ANGLE

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code OLO·November 10, 2017

HIP END EFFECTOR, VARIABLE ANGLE

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code OLO·August 29, 2017

HIP END EFFECTOR, VARIABLE ANGLE

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code OLO·August 2, 2017

HIP END EFFECTOR, VARIABLE ANGLE

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code OLO·November 10, 2017