82 results · 25ms · Sources: EU EUDAMED, US FDA

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Flexor Tuohy-Borst Side-Arm Introducers Shuttle Select

FDA 510(k)
FDA Class 2 ·Cardiovascular

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Injury ·COOK INC·Product code DYB·October 29, 2025

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Injury ·COOK INC·Product code DYB·October 29, 2025

DYB INTRODUCER, CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code DYB·November 12, 2025

FLEXOR SHUTTLE SELECT GUIDING SHEATH

FDA Adverse Event
Injury ·COOK INC·Product code DYB·October 29, 2025

UNKNOWN

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·September 15, 2020

FLEXOR SHUTTLE SELECT GUIDING SHEATH

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·February 7, 2020

Ophthalmic Speculum

FDA UDI
KATENA PRODUCTS, INC.·00841668100318·ALPHONSO INFANT SPECULUM

Ophthalmic Speculum

FDA UDI
KATENA PRODUCTS, INC.·00841668100301·INFANT WIRE SPECULUM 3MM/5MM BLADES

Sklar®

FDA UDI
SKLAR CORPORATION·10649111072321·SKLARHONE MAYO SCIS CV SERR5.5

PROULTRA PIEZO ULTRASONIC

FDA 510(k)
FDA Class 2 ·Dental

TONO-PEN AVIA TONOMETER AND OCU-SHILED TIP COVER

FDA 510(k)
FDA Class 2 ·Ophthalmic

ARCHITECT SYPHILIS TP REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LIP·April 8, 2026

ARCHITECT SYPHILIS TP REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LIP·May 1, 2026

ALINITY I SYPHILIS TP REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LIP·May 4, 2026

ALINITY I SYPHILIS TP REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LIP·May 22, 2026

COMPLETE REVITALENS

FDA Adverse Event
Malfunction ·ABBOTT MEDICAL OPTICS·Product code LPN·October 8, 2014

SPRINT

FDA Adverse Event
Injury ·MPRI·Product code LWS·June 8, 2013

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 21, 2011

ALINITY I SYPHILIS TP REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LIP·April 13, 2026