K810211

FDA 510(k)

FDA Class 2 ·Clinical Chemistry

FDA UDI

MEDI MANUFACTURING, INC.·04051526743458·LEVAMED ANKLE SUPPORT SILVER I

FDA UDI

OXOID LIMITED·05032384502950·

FDA UDI

LANCER ORTHODONTICS, INC.·00817573022892·PORCELAIN CONDITIONER LANCER

FDA UDI

Kalitec Direct LLC·B07312K0102110·Shaver, Open 11mm

FDA UDI

XENIX MEDICAL LLC·00818345023949·PADDLE SPREADER, 11MM

FDA UDI

NEXTSTEP ARTHROPEDIX, LLC·00816127020421·Neck Trial, Size 11, Lateral

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

FDA 510(k)

FDA Class 1 ·General Hospital

FDA Adverse Event

Malfunction ·WELCH ALLYN PROTOCOL, INC.·Product code DSI·February 5, 2014

FDA Adverse Event

Malfunction ·CORDIS NEUROVASCULAR, INC.·Product code KRA·October 31, 2012

FDA Adverse Event

Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 2, 2015