27 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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VerteLP Interbody Fusion Device
FDA 510(k)
FDA Class 2
·Orthopedic
Eagle Derma2 Nitrile Examination Gloves
FDA UDI
Eagle Protect Pbc·09421024254131·Derma2 Nitrile Examination Gloves, Blue, Powder...
DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169502208·INTERBODY 2151312 LARGE - 6 DEG 12MM
Oticon
FDA UDI
Oticon A/S·05707131288783·H11V2, DESIGNRITE 10 WL CRED
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311513120·
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321513120·
ATTUNE
FDA UDI
DEPUY (IRELAND)·10603295043584·ATTUNE KNEE SYSTEM REVISION PRESSFIT STEM 12X160MM
HNM SPORTS MEDICINE
FDA UDI
HNM STAINLESS, LLC.·00842962101575·ETHOS PRO LABRAL ANCHOR, TITANIUM, 2.9mm x 6mm,...
ATTUNE
FDA UDI
DEPUY (IRELAND)·10603295043546·ATTUNE KNEE SYSTEM REVISION PRESSFIT STEM 12X60MM
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575289233·Orthopaedic implant aiming/guiding block, reusa...
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575289264·Orthopaedic implant aiming/guiding block, reusa...
ATTUNE
FDA UDI
DEPUY (IRELAND)·10603295043553·ATTUNE KNEE SYSTEM REVISION PRESSFIT STEM 12X110MM
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575289240·Orthopaedic implant aiming/guiding block, reusa...
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575289288·Orthopaedic implant aiming/guiding block, reusa...
NUVUE COLORMARK9TM) NEEDLE
FDA 510(k)
FDA Class 2
·Radiology
SWIRLGRAFT BYPASS AND VASCULAR ACCESS GRAFTS
FDA 510(k)
FDA Class 2
·Cardiovascular
HNM SPORTS MEDICINE
FDA UDI
HNM STAINLESS, LLC.·00842962103647·ETHOS PRO LABRAL ANCHOR, TITANIUM, 2.9mm x 6mm,...
EXPECT PULMONARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·May 19, 2026
EXPECT PULMONARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·September 24, 2025
ACQUIRE? PULMONARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·October 10, 2025