22 results
·
31ms
·
Sources: EU EUDAMED, US FDA
OLDELFT THORASCAN MODEL NUMBER 180T
FDA 510(k)
FDA Class 2
·Radiology
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040017357·Zirlux 16+ D98,5*30 (step) A3
36M - UP Facilities - Metal
FDA UDI
Certified Safety Manufacturing, Inc.·00766588121659·36M - UP Facilities - Metal
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033359068·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033359075·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033359013·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033359020·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033359051·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033359037·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033359044·
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197026505·Standard Operating Scissors Fig. 2
straig...
LINEZOLID, 30UG, BBL SENSI-DISC
FDA 510(k)
FDA Class 2
·Microbiology
ERO SCAN OAE TEST SYSTEM
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·March 13, 2013
ADJ. X-CONN. MEDIUM 45-60.5MM
FDA Adverse Event
Malfunction
·THEKEN SPINE·Product code NKB·February 1, 2011
FREESTYLE
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC.·Product code LFR·May 16, 2007
MULTI-LINK 8
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code MAF·June 4, 2010
MULTI-LINK 8
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code MAF·June 4, 2010
UNKNOWN GST RELOAD
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 1, 2025
UUltrasound System 2300, bkActiv w/battery; Model No. 2300-11; System, Imaging, Pulsed Doppler, Ultrasonic
FDA Enforcement
Class II
·Ongoing·B-K Medical A/S·November 12, 2025