K090106

FDA 510(k)

FDA Class 2 ·Dental

FDA UDI

Zest Anchors, LLC·00840481119583·LOCATOR, F-Tx Attachment System, Regular Platfo...

FDA UDI

Zest Anchors, LLC·00840481113826·LOCATOR R-Tx Abutment for Regular Internal Conn...

FDA UDI

LEONE SPA·08033707065630·INTRAORAL ELASTICS 2,5 oz 1/8" brown

FDA UDI

Kalitec Direct LLC·B07323K0101060·Distractor, Smooth Paddle, Lordotic, 6mm

FDA UDI

Kalitec Direct LLC·B07312K0101060·Distractor, Smooth Paddle, 6mm

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

FDA 510(k)

FDA Class 2 ·Cardiovascular

FDA Adverse Event

Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 2, 2013

FDA Adverse Event

Malfunction ·MINDRAY DS USA, INC.·Product code MHX·August 18, 2014

FDA Adverse Event

Injury ·MEDTRONIC MINIMED·Product code LZG·May 5, 2011

FDA Adverse Event

Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026

FDA Adverse Event

Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

FDA Adverse Event

Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026

FDA Adverse Event

Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026