23 results · 19ms · Sources: EU EUDAMED, US FDA

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SALINE IV FLUSH SYRINGE

FDA 510(k)
FDA Class 2 ·General Hospital

artVeneer life

FDA UDI
Merz Dental GmbH·D7092002142·artVeneer life upper posteriors, L, D3

SCANLAN®

FDA UDI
SCANLAN INTERNATIONAL INC·00846159018189·Vascular Clamp Straight Jaw

Metal Custom Rx

FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746102486·BRACKET SINGLE WIDTH 022 TQ=0 A=0 R=0 PROFILE=S...

CURE OPEL-L (S)

FDA UDI
MEDITECH SPINE, LLC·B167900021420·

OPEL-L

FDA UDI
SpineArt SA·07640332477205·OPEL-L PLATE ASSEMBLY, L42

CURE OPEL-L (S)

FDA UDI
MEDITECH SPINE, LLC·B167S1900021420·

AUDIO TECHNOLOGIES S:R.1

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

MIDAS TOUCH LATEX EXAMINATION GLOVES-POWDER FREE

FDA 510(k)
FDA Class 1 ·General Hospital

16PW - Norfolk Southern 002142-0 - Poly White

FDA UDI
Certified Safety Manufacturing, Inc.·00766588170077·16PW - Norfolk Southern 002142-0 - Poly White

Z.S.G.M. CUTTER 2:1 RATIO ( CAUTION: SHARP )

FDA Adverse Event
Malfunction ·ZIMMER SURGICAL, INC.·Product code FZW·August 28, 2023

HEARTSINE SAMARITAN 300P AND PAD PAK

FDA Adverse Event
Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·February 11, 2013

UNKNOWN DEPUY ASR HIP

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 18, 2011

840 VENTILATOR

FDA Adverse Event
Malfunction ·PURITAN - BENNETT CORP.·Product code CBK·February 25, 2008

TRULIANT PS CEM FEM PS CEM RIGHT SZ 6

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·October 12, 2023

VOYANT® FINE FUSION DEVICE

FDA Adverse Event
Injury ·APPLIED MEDICAL RESOURCES·Product code GEI·August 29, 2024

VOYANT® FINE FUSION DEVICE

FDA Adverse Event
Injury ·APPLIED MEDICAL RESOURCES·Product code GEI·August 29, 2024

VOYANT® FINE FUSION DEVICE

FDA Adverse Event
Injury ·APPLIED MEDICAL RESOURCES·Product code GEI·August 29, 2024

VOYANT® FINE FUSION DEVICE

FDA Adverse Event
Injury ·APPLIED MEDICAL RESOURCES·Product code GEI·August 29, 2024

Smiths Medical, Medfusion¿ Syringe Infusion Pump, Model 4000, Software Version V1.0 & V1.1, Reorder Numbers 4000-0100-50, 4000-0100-95, 4000-0101-50, 4000-0101-51, and 4000-0101-78. Designed for use in care areas for the administration of fluids requiring precisely controlled infusion rates.

FDA Enforcement
Class I ·Terminated·Smiths Medical ASD, Inc.·August 8, 2012