21 results
·
18ms
·
Sources: EU EUDAMED, US FDA
AP-1 AUTO PROGRAMMER
FDA 510(k)
FDA Class 1
·Physical Medicine
BR2000 BLADES
FDA UDI
Peter Brasseler Holdings, LLC·00887919100812·K7-2590-47
Brasseler
FDA UDI
Provision·B504OMK72590500·
Brasseler
FDA UDI
Provision·B504OMK72590470·
CURA 778
FDA 510(k)
FDA Class 2
·Radiology
PDS PLATES
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
NA
FDA UDI
STERILMED, INC.·10888551007511·SAW BLADE OSCILLATING AGGRESSIVE CUT LARGE BONE
NA
FDA UDI
STERILMED, INC.·10888551007580·SAW BLADE SAGITTAL K9 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007573·SAW BLADE SAGITTAL FLARED K9 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007504·SAW BLADE OSCILLATING AGGRESSIVE CUT LARGE BONE
NA
FDA UDI
STERILMED, INC.·10888551007559·SAW BLADE SAGITTAL K9 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007566·SAW BLADE SAGITTAL K9 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007603·SAW BLADE SAGITTAL K9 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007597·SAW BLADE SAGITTAL K9 K2000 SERIES
TRULIANT TIB IMP PS INSERT SZ 2.5 11MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·August 19, 2022
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 20, 2014
PINNACLE MTL INS NEUT36IDX58OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·October 16, 2012
VIRTUOSO DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code LWS·August 11, 2010
VERSA-DIAL SHOULDER SYSTEM HUMERAL HEAD TRIAL
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code HWT·June 28, 2017
Azurion 7 M12; Catalog numbers: (1) 722078, (2) 722223, (3) 722233 (OUS ONLY).
FDA Enforcement
Class I
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025