157 results · 31ms · Sources: EU EUDAMED, 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