K033908

FDA 510(k)

FDA Class 2 ·Immunology

FDA UDI

Merz Dental GmbH·D7091033908·Baltic Denture System BDLoad BDLoad Mm7 PLSEbi...

FDA UDI

ALFA SCIENTIFIC DESIGNS, INC.·10796918001310·INSTANT-VIEW Multi-Drugs of Abuse Urine Test AM...

FDA UDI

Kalitec Direct LLC·B07311K0330080·Rocker, Hinged, Locking

FDA 510(k)

FDA Class 2 ·Dental

FDA 510(k)

FDA Class 2 ·General Hospital

FDA Adverse Event

Malfunction ·INVACARE SUZHOU·Product code BTI·April 3, 2013

FDA Adverse Event

Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·March 23, 2011

FDA Adverse Event

Injury ·KALTENBACH & VOIGT GMBH·Product code EKX·April 24, 2008

FDA Adverse Event

Malfunction ·MASIMO CORPORATION·Product code DQA·July 10, 2015

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