360 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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K2M Growing Spine System
FDA 510(k)
FDA Class 2
·Orthopedic
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16721610280·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1672161028060·
XENMATRIX
FDA UDI
Davol Inc.·00801741031403·XenMatrix Surgical Graft, 10 cm x 28 cm (3.9” x...
ORTHOPEDIC SALVAGE SYSTEM (OSS)
FDA UDI
Biomet Orthopedics, LLC·00880304250895·
CARDINAL HEALTH
FDA UDI
Cardinal Health 200, LLC·10885425499106·STAPLE REMOVER
Symmetry Rochester-Pean
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482056011·Symmetry® Forceps, Rochester-Pean Hemostatic, S...
Pinehurst Anterior Cervical Plate System
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215030643·
Aquila Anterior Cervical Plate System
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215125707·
EUS BALLOON
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PRECISION THUNIS 800+
FDA 510(k)
FDA Class 2
·Radiology
PRADO™ Lumbar Interbody Fusion System
FDA UDI
Pt. Solutions, LLC·G616RTFH161028150·NON-STERILE PRADO™ T HA PEEK IBF, 16MM H X 10MM...
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017