11 results · 27ms · 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.

MAXI-NEB

FDA 510(k)
FDA Class 1 ·Anesthesiology

Sklar®

FDA UDI
SKLAR CORPORATION·10649111223525·GUYON SOUND W/THREAD 27FR

NAR

FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209110155·

IFS Fixation Scaffold System

FDA 510(k)
FDA Class 2 ·Orthopedic

Lyme-ID IgG Test; Bio-ID800

FDA 510(k)
FDA Class 2 ·Microbiology

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2014

VITALITY

FDA Adverse Event
Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 4, 2010

PSI KIT: 8.5 FR X 4-1/8 (10 CM)

FDA Adverse Event
Malfunction ·ARROW INTL., INC.·Product code DYB·November 14, 2012

Allura Xper FD20 Product Codes: (1)722012, (2) 722028, (3) 722006; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;

FDA Enforcement
Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·October 1, 2025

Exactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Left, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-22, b) 41, 44, 47, 50, head, Medium, Item Number 314-13-23, c) 44, 47, 50, 53 head, Large, Item Number 314-13-24, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-13-25; Shoulder Arthroplasty

FDA Enforcement
Class II ·Ongoing·Exactech, Inc.·April 10, 2024

DATEX-OHMEDA S/5 SINGLE-WIDTH AIRWAY MODULE, E-MINIC AND ACCESSORIES. DATEX-OHMEDA S/5TM FM WITH L-FICU04 ANDL-FICUO4A SOFTWARE AND N-FCREC MODULE **(OUS only). E-miniC and accessories is indicated for monitoring C02 and respiration rate of all hospital patients.

FDA Enforcement
Class I ·Terminated·GE Healthcare, LLC·July 30, 2014