45 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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WAVELIGHT FS200 LASER SYSTEM MODEL: FS200
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
KENAFLEXX
FDA UDI
KENTRON HEALTHCARE, INC.·00852244007198·I.V. ADMINISTRATION SET 10 DROPS WITH 2 CONNECT...
RINGLOC TRI-SPIKE HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304184480·
n/a
FDA UDI
Ortho Development Corporation·00822409088935·Modular Straight Inserter
Altus Spine Cervical Interbody Fusion System
FDA UDI
Altus Spine, LLC·00843210131030·ALR Sizer W/Tab
EVOS Lumbar Interbody System
FDA UDI
Cutting Edge Spine, LLC·00841193107905·HA PEEK EVOS Straight, ,6mmx8mmx 26mm , FLAT 0...
ALL SILICONE FOLEY BALLOON CATHETER
FDA UDI
Sewoon Medical Co., Ltd.·08806369402002·2way/Translucent 1.5cc 6fr
OsteoMed
FDA UDI
OSTEOMED LLC·00845694048835·PrimaLIF Radial Clamp
UCR
FDA UDI
Seaspine Orthopedics Corporation·10889981029371·ROD, 5.5 X 60MM
Air-Q®
FDA UDI
AIRLIFE·10889483214121·STYLET AIR-Q SIZE #00 DISPOSABLE LARYNGEAL AIRW...
COMPLETE MOISTURE PLUS
FDA Adverse Event
Injury
·AMO·Product code LPN·December 17, 2006
THERATRON 780C/1000 WITH COMPUTERIZED CONSOLE UPGRADE
FDA 510(k)
FDA Class 2
·Radiology
AMYSEAT TILT/RECLINE SEATING
FDA 510(k)
FDA Class 2
·Physical Medicine
Inserter-Retriever
FDA UDI
BICON, LLC·00813110023827·3.0mm Long Implant Inserter/Retriever
Intervertebral Body Fusion Device
FDA UDI
PRECISION SPINE, INC.·00840019922227·Sizer Inserter (10-1018 Handle)
ELECTRONIC GAS BLENDER
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DTX·November 19, 2025
STOCKERT S3 GAS BLENDER
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·December 22, 2014
OT VERIO PRO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 8, 2013
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·September 19, 2014
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 24, 2011