157 results
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31ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ClearUP Sinus Pain Relief
FDA 510(k)
FDA Class 2
·Neurology
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X1820250·18mm H x 20mm W x 25mm L x 0 degrees XLIF
SSW CARBIDE GREAT WHITE
FDA UDI
Ss White Burs, Inc.·D6901820252·GREAT WHITE GOLD CARBIDE GW2 ROUND - 5 PACK
Vilex Power Accessory
FDA UDI
VILEX IN TENNESSEE, INC.·00841731122292·Kwire .070X9" (1.8x225mm)
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L182025120·18mm H x 20mm W x 25mm L XLIF Trial 12 degree L...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X18202580·18mm H x 20mm W x 25mm L x 8 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X182025120·18mm H x 20mm W x 25mm L x 12 degrees XLIF
RIVERPOINT BRACHYTHERAPY
FDA UDI
RIVERPOINT MEDICAL, LLC·00812444020472·BRACHYTHERAPY
Coxa Vara DAA Trial Neck
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215055806·
RIVERPOINT BRACHYTHERAPY
FDA UDI
RIVERPOINT MEDICAL, LLC·00812444022261·BRACHYTHERAPY
BODY-JET
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
COMBAT READY CLAMP
FDA 510(k)
FDA Class 2
·Cardiovascular
BRACHYTHERAPY
FDA UDI
RIVERPOINT MEDICAL, LLC·00812444024975·BRACHYTHERAPY
BD BBL¿ THIOGLYCOLLATE MEDIUM, ENRICHED WITH VITAMIN K1 AND HEMIN
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code JSG·April 14, 2022
CENTRELLA BED
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FNL·April 25, 2026
CORE IMPACTION DRILL
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code DZJ·June 21, 2013
SILICONE ADVANCED OPTIC-VIOLET SHIELD
FDA Adverse Event
Malfunction
·BAUSCH & LOMB·Product code HQL·September 22, 2008
SECURE 3 MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·June 22, 2011
SYNCHROMED II
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·April 22, 2025
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·December 20, 2024