23 results · 22ms · Sources: EU EUDAMED, US FDA

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RS ORANGE NITRILE MEDICAL EXAMINATION GLOVES (POWDER FREE)

FDA 510(k)
FDA Class 1 ·General Hospital

Oticon

FDA UDI
Oticon A/S·05707131260925·RIA, MINIRITE 312 WL STG

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613070748·Metzenbaum (Lahey) Scissors, Super Cut, Curved,...

SONOSENS

FDA 510(k)
FDA Class 2 ·Orthopedic

DOSEVIEW 3D

FDA 510(k)
FDA Class 2 ·Radiology

SLEEPSTYLE AUTO

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZD·January 2, 2025

SLEEPSTYLE AUTO

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZD·February 18, 2025

SLEEPSTYLE AUTO

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZD·September 12, 2024

M.U.S.T. PEDICLE SCREW 7X45

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MNI·January 20, 2017

SLEEPSTYLE AUTO

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZD·November 14, 2024

PEDICLE SCREW 03.50.030 PEDICLE SCREW 7X40

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·February 3, 2020

SECURE II MED/SURG BED

FDA Adverse Event
Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·May 29, 2013

SECURE 3 MED/SURG BED

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FNL·May 4, 2011

MONOCRYL (POLIGLECAPRONE 25) SUTURE

FDA Adverse Event
Injury ·ETHICON, INC.·Product code GAN·August 21, 2008

MECTALIF POSTERIOR

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·October 8, 2025

MECTALIF OBLIQUE INTERBODY FUSION DEVICE PEEK/TI 12X28X7 L0°

FDA Adverse Event
Malfunction ·MEDACTA INTERNATIONAL SA·Product code MAX·November 10, 2017

MECTALIF (TI PEEK) POSTERIOR INTERBODY FUSION DEVICE PEEK/TI 11X22X7 L5

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·April 29, 2020

MECTALIF ANTERIOR STAND-ALONE SCREW DIAM.5X30 LONG HEAD

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code OVD·May 23, 2019

MECTALIF POSTERIOR (TI PEEK) POSTERIOR INTERBODY FUSION DEVICE PEEK/TI

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·May 25, 2023

PEDICLE SCREW PEDICLE SCREW 6X40

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·September 21, 2018