31 results · 38ms · Sources: EU EUDAMED, US FDA

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MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526550162·GENUMEDI PT KNEE SUP SILVER L EW VII

Reliance Interspinous Plate System

FDA 510(k)
FDA Class 2 ·Orthopedic

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526550131·GENUMEDI PT KNEE SUP SILVER L EW IV

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526550124·GENUMEDI PT KNEE SUP SILVER L EW III

SYSTEM 1E CHEMICAL INDICATOR

FDA 510(k)
FDA Class 2 ·General Hospital

FLOWMEDIC, MODEL 220

FDA 510(k)
FDA Class 2 ·Cardiovascular

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·March 23, 2023

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523156665·Tesera-k ALIF, 42W X 32D, 17mm, 12° Trial

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523163663·PEEK ALIF Implant 42 X 32, 17mm Height, 17° Lor...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138661·Broach, 42 X 32, 17mm Height 17° Hyperlordotic

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523152230·Tesera-k SA, 42mm X 32mm X 17mm, 12° Lordosis, T3

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523157419·Tesera-k ALIF, 42W X 32D, 17mm, 12° Broach

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523137763·Trial, 42 X 32, 17mm Height 17° Hyperlordotic

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523136650·Ti-6Al-4V ALIF Implant 42 X 32, 17mm Height 17°...

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·July 14, 2021

VANTAGE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code HSN·March 25, 2019

VANTAGE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code HSN·March 25, 2019

VANTAGE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code HSN·June 3, 2019

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 5, 2014

QUATTRODE

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 29, 2013