34 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CROSSEAL APPLICATION DEVICE
FDA 510(k)
FDA Class 2
·General Hospital
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00885074163826·CASE 7030032 SCREW GAUGE
STAR
FDA UDI
Stryker GmbH·00886385017068·RASP ASSEMBLY
Humelock Reversed Shoulder
FDA UDI
FX SOLUTIONS·03701037307229·HUMELOCK REVERSED EXTRACTOR
SCFE Screw
FDA UDI
ORTHOPEDIATRICS CORP.·00841132114155·4.0mm X 32mm MED THREAD CANNULATED SCREW
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710420300320·Anterio Lateral Closing Wedge Osteotomy Guide, ...
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710410300320·Anterior Closing Wedge Osteotomy Guide, 30mm x ...
UNKNOWN MESH PRODUCT (EWHU)
FDA Adverse Event
Injury
·ETHICON INC·Product code FTL·September 9, 2011
SEED SELECTRON MODEL V. 1.0
FDA 510(k)
FDA Class 2
·Radiology
LEVEEN NEEDLE ELECTRODE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·HYLAFORM (HYLAN B GEL)
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·PREVELLE SILK
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·HYLAFORM, HYLAFORM PLUS, ND CAPTIQUE
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·HYLAFORM AND HYLAFORM PLUS
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·PREVELLE SILK
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·PREVELLE SILK
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·HYLAFORM PLUS (HYLAN B GEL)
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·HYLAFORM (HYLAN B GEL), HYLAFORM PLUS, CAPTIQUE
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·PREVELLE SILK & HYLAN B GEL
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·HYLAFORM (HYLAN B GEL); PREVELLE SILK