16 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.

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772814275·GENUMEDI PT SILVER R IV

TrueBeam-TrueBeam STx-Edge

FDA 510(k)
FDA Class 2 ·Radiology

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772814213·GENUMEDI PT SILVER L IV

Galaxy

FDA UDI
DIOMEDICAL CO.,LTD.·08809263396705·Galaxy ACIF cage H14 x W32 x L24

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613097844·Vienna Nasal Speculum, Number 3, 33m Convention...

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587A143224120·14mm H x 32mm W x 24mm L x 12 degrees ALIF

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587A14322480·14mm H x 32mm W x 24mm L x 8 degrees ALIF

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587A143224150·14mm H x 32mm W x 24mm L x 15 degrees ALIF

GEN-PROBE APTIMA COMBO 2 ASSAY

FDA 510(k)
FDA Class 2 ·Microbiology

HOSPIRA PLUM INFUSION SET; HOSPIRA INFUSION SET WITH YELLOW STRIPE TUBING

FDA 510(k)
FDA Class 2 ·General Hospital

EQUINOXE

FDA Adverse Event
Other ·EXACTECH INC·Product code HSD·May 28, 2013

VERSACARE

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code FNL·September 3, 2008

ACCU-CHEK ® COMPACT TEST DRUM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 28, 2011

4.5 BROAD SCP PLT 26-H STER

FDA Enforcement
Class II ·Terminated·Zimmer Biomet, Inc.·June 21, 2017

RESTORE ADVANCED

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 29, 2013

Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);

FDA Enforcement
Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026