22 results · 23ms · Sources: EU EUDAMED, US FDA

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UNDUS MALE LATEX CONDOM (WITH FLAVORING)

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

Ophthalmic Cannula

FDA UDI
KATENA PRODUCTS, INC.·00841668114063·MCINTYRE-BINKHORST CAN 25GA ANG RT PK/10

NA

FDA UDI
STERILMED, INC.·10888551019842·SAW BLADE MICRO OSCILLATING CRESCENTIC 32MM CUT...

NA

FDA UDI
STERILMED, INC.·10888551017831·SAW BLADE MICRO OSCILLATING CRESCENTIC 32MM CUT...

CONMED

FDA UDI
Conmed Corporation·10845854002254·MICRO OSCILLATOR BLADE, CRESCENTIC, 13.5 X 32 X...

BIOEMG II AND BIOJVA

FDA 510(k)
FDA Class 2 ·Physical Medicine

MODIFICATION TO: SENS-A-RAY SYSTEM WITH PROIMAGE SOFTWARE

FDA 510(k)
FDA Class 2 ·Dental

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

INNOVA 4100

FDA Adverse Event
Malfunction ·GE MEDICAL SYSTEMS·Product code MQB·April 4, 2011

INNOVA 4100

FDA Adverse Event
Malfunction ·GE MEDICAL SYSTEMS·Product code MQB·May 6, 2011

AIR DERMATOME HANDPIECE

FDA Adverse Event
Malfunction ·ZIMMER SURGICAL·Product code GFD·February 27, 2013

TOTALCARE

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FNL·February 15, 2011

COLLEAGUE CX VOLUMETRIC INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·April 4, 2008