17 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ZONARE ZS3 and Z.Onepro Diagnostic Ultrasound System
FDA 510(k)
FDA Class 2
·Radiology
AGXO
FDA UDI
Oticon A/S·05707131286246·H160V2 TI, RITE 312 WL SIL AGXO
Vilex Guidewire
FDA UDI
VILEX IN TENNESSEE, INC.·00841731120588·Guidewire 2.4x150mm Sgl Trocar
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100141·KRATZ-BARRAQUER HEAVY WIRE SPECULUM
S-LIFT®
FDA UDI
SPINEFRONTIER, INC.·00190361038412·TRIAL RASP, STRAIGHT, 19MM WIDE, 12MM
S-LIFT®
FDA UDI
SPINEFRONTIER, INC.·00190361038399·TRIAL RASP, STRAIGHT, 19MM WIDE, 8MM
S-LIFT®
FDA UDI
SPINEFRONTIER, INC.·00190361038382·TRIAL RASP, STRAIGHT, 19MM WIDE, 6MM
S-LIFT®
FDA UDI
SPINEFRONTIER, INC.·00190361038429·TRIAL RASP, STRAIGHT, 19MM WIDE, 14MM
S-LIFT®
FDA UDI
SPINEFRONTIER, INC.·00190361038405·TRIAL RASP, STRAIGHT, 19MM WIDE, 10MM
Patella Trial Size 4
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215074142·
HL168JP
FDA 510(k)
FDA Class 2
·Cardiovascular
TROJAN MAGNUM CONDOM WITH WARMING LUBRICANT
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
TROJAN PLEASURE PACK LUBRICATED CONDOMS
FDA Adverse Event
Injury
·CHURCH & DWIGHT CO., INC.·Product code HIS·October 29, 2014
UNKNOWN HIP FEMORAL HEAD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWY·June 6, 2013
SM204 M-SERIES W/BIG WHEEL
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·June 10, 2011
SYNCHROMED II
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·September 3, 2008
MEDTRONIC DUAL CHAMBER TEMPORARY EXTERNAL PACEMAKER 510(K) K150246
FDA Adverse Event
Death
·MEDTRONIC, INC.·Product code DTE·February 10, 2021