23 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
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