15 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Disposable Endoscopic Bipolar
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BD BBL™ Sensi-Disc™ Mezlocillin - 75 µg
FDA UDI
BECTON, DICKINSON AND COMPANY·30382902316153·BD BBL™ Sensi-Disc™ Mezlocillin 75 µg
3D Printed Interbody Systems
FDA UDI
Seaspine Orthopedics Corporation·10889981304096·2-Hole No-Profile Interbody, 39mm x 30mm x 16mm...
Meridian
FDA UDI
Seaspine Orthopedics Corporation·10889981309978·Trial Rasp, 39mm x 30mm x 16mm, 15 Deg
Meridian
FDA UDI
Seaspine Orthopedics Corporation·10889981215668·No-Profile Interbody, 39mm x 30mm x 16mm, 15 Deg
SLED CURING LIGHT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
POLARIS SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523157440·Tesera-k ALIF, 31W X 26D, 15mm, 17° Broach
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523156696·Tesera-k ALIF, 31W X 26D, 15mm, 17° Trial
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523151622·Tesera-k SA, 31mm X 26mm X 15mm, 17° Lordosis, T3
KEOFEED TUBE
FDA Adverse Event
Injury
·CORPAK·Product code KNT·October 31, 2014
6 SHOOTER SAEED MULTI-BAND LIGATOR
FDA Adverse Event
Malfunction
·WILSON-COOK MEDICAL INC.·Product code MND·August 15, 2011
PELVICOL 2CM X 7CM 1.0MM
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY TISSUE·Product code FTL·July 12, 2013
CLAVICLE FRACTURE PLATE, CENTRAL THIRD, RIGHT, STAINLESS STEEL
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HTN·July 7, 2017
Revogene, Catalog no. 610210. IVD test instrument
FDA Enforcement
Class II
·Ongoing·Meridian Bioscience Inc·August 3, 2022