21 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ARIX Rib System
FDA 510(k)
FDA Class 2
·Orthopedic
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676221412150·
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676221412000·
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676221412070·
N/A
FDA UDI
PENTAX OF AMERICA, INC.·04961333242658·CABLE FOR FUJIFILM PROCESSORS
V2 TRIVERSE IMPACTOR TIBIAL
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215127626·
Empower Clear Bracket
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746200625·COSMETIC SL EMPOWER CLEAR INTERACT UR BIC 022 T...
Empower Clear
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746021428·COSMETIC SL EMPOWER CLEAR INTERACT UR BICUSPID ...
Empower Clear
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746154416·COSMETIC SL EMPOWER CLEAR INTERACT UR BIC 022 T...
PAX-FLEX3D, PHT-7000
FDA 510(k)
FDA Class 2
·Radiology
LATEX EXAMINATION GLOVES, POWDER FREE, POLYMER COATED
FDA 510(k)
FDA Class 1
·General Hospital
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·August 30, 2023
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 13, 2025
Unison®-C Anterior Cervical Fixation System
FDA UDI
Pioneer Surgical Technology, Inc.·00846468083205·Interbody Fusion Device, 22mm (W), 16mm (D), 12...
Unison®-C Anterior Cervical Fixation System
FDA UDI
Pioneer Surgical Technology, Inc.·00846468083274·Interbody Fusion Device, 22mm (W), 16mm (D), 12...
Unison®-C Anterior Cervical Fixation System
FDA UDI
Pioneer Surgical Technology, Inc.·00846468081669·Trial, 22mm (W), 14mm (D), 12mm (H), 7° Lordosis
Unison®-C Anterior Cervical Fixation System
FDA UDI
Pioneer Surgical Technology, Inc.·00846468082222·Rasping Trial, 22mm (W), 14mm (D), 12mm (H), 7°...
LIGASURE IMPACT
FDA Adverse Event
Malfunction
·COVIDIEN LLC (SHANGHAI)·Product code GEI·June 28, 2013
3.5MM 90 DEGREE SERFAS ENERGY PROBE
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY PUERTO RICO·Product code GEI·August 16, 2011
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·November 3, 2014