112 results · 21ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

GLUCOSTABILIZER INSULIN DOSING CALCULATOR

FDA 510(k)
FDA Class 2 ·Anesthesiology

SCHWERT

FDA UDI
A. Schweickhardt GmbH & Co. KG·E8961413210·Periosteal elevators 6mm

VEROSCOPE OPTICAL VERESS CANNULA & DILATION TUBE SYSTEM

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

EMATRIX CO2

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

POSIFLUSH

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·April 20, 2026

POSIFLUSH

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 1, 2026

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·March 14, 2018

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·August 10, 2017

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·August 10, 2017

BD POSIFLUSH

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code NGT·March 20, 2026

BD POSIFLUSH

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code NGT·March 20, 2026

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·February 22, 2018

BD POSIFLUSH NORMAL SALINE SYRINGE

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·January 6, 2021

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·July 13, 2017

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·July 13, 2017

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 5, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 5, 2019

OCTRODE

FDA Adverse Event
Injury ·ST. JUDE MEDICAL NEUROMODULATION·Product code LGW·May 24, 2013

LTV 900

FDA Adverse Event
Malfunction ·CAREFUSION 203, INC·Product code CBK·June 1, 2011

530G INSULIN PUMP

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·October 3, 2014