55 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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XLP - CPRotector® Deluxe - Orange Nylon Pouch
FDA UDI
Certified Safety Manufacturing, Inc.·00766588030067·XLP - CPRotector® Deluxe - Orange Nylon Pouch
R2 Dermabrasion Tip (for Dermal Cooling System)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
NuVasive
FDA UDI
Nuvasive, Inc.·00887517184412·XLIF Dilator, 6mm Thoracic
EVOS Lumbar Interbody System
FDA UDI
Cutting Edge Spine, LLC·00841193113494·HA PEEK EVOS Straight, ,6mmx9mmx 22mm , FLAT 0...
NA
FDA UDI
Stryker GmbH·07613154639908·Screw Marker 30,6
TWO-LUMEN PICC WITH BLUE FLEXTIP CATHETER AND INTEGRAL NEEDLE PROTECTION
FDA 510(k)
FDA Class 2
·General Hospital
CentriMag Circulatory Support System, CentriMag Return (Arterial) Cannula Kit, CentriMag Drainage (Venous) Cannula Kit
FDA 510(k)
FDA Class 2
·Cardiovascular
BARD® URINARY DRAINAGE BAG
FDA Adverse Event
Malfunction
·C. R. BARD, INC.·Product code KNX·December 11, 2025
BD LUER-LOK
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY·Product code FMF·January 21, 2026
MECTACER BIOLOX DELTA FEMORAL BALL HEAD
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·December 18, 2025
XtraFix®
FDA UDI
Zimmer, Inc.·00889024080607·
XtraFix®
FDA UDI
Zimmer, Inc.·00889024080621·
XtraFix®
FDA UDI
Zimmer, Inc.·00889024080614·
XtraFix®
FDA UDI
Zimmer, Inc.·00889024080584·
XtraFix®
FDA UDI
Zimmer, Inc.·00889024080577·
XtraFix®
FDA UDI
Zimmer, Inc.·00889024080591·
FLUID DISPENSING CONNECTOR
FDA Adverse Event
Malfunction
·B. BRAUN MEDICAL INC.·Product code KYX·January 23, 2026
LUER-LOK
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMF·February 9, 2026
MECTACER BIOLOX DELTA FEMORAL BALL HEAD
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·December 18, 2025
BD SYRINGE 3ML LL BNS
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·September 11, 2025