15 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STRAUMANN(R) VARIOBASE(TM) ABUTMENT NNC, STRAUMANN(R) VARIOBASE(TM) ABUTMENT RN, STRAUMANN(R) VARIOBASE(TM) ABUTMENT WN,
FDA 510(k)
FDA Class 2
·Dental
Peerless Buccal Tube
FDA UDI
ORMCO CORPORATION·00889989053630·ORTHOS LSM 6DG -10T B/T NDX LL 22
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613052812·Infusion Handle, Delron, Male To Female Connect...
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613069094·Scleral Plug Forceps, Small Cup Shape In The In...
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613098148·Infusion Cannula, 20ga, 6mm Tip
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613088057·I/A Handpiece, 17GO, 23GI, 0.3mm, Straight
COMPREHENSIVE LOCKING SCREW
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HWC·July 5, 2019
REVOLUTION SPINAL FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SOCORRO SMI TUNNEL RELEASE DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
S4 IMPLANTS
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code KWP·August 29, 2008
FUJIFILM 600 SERIES ENDOSCOPE EC-600WM
FDA Adverse Event
Malfunction
·FUJIFILM CORPORATION·Product code FDF·January 22, 2025
NAIL HANDLE T2 FEMUR
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS-KIEL·Product code LXH·May 29, 2013
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·June 14, 2011
VITALITY 2
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 1, 2014
Ultraview SL Command Modules, Model 91496, with the Masimo SpO2 PCBA, PN: 010-1636-02. The Spacelabs Multi-parameter Module is intended for use with the Patient Care Management System (PCMS) to acquire, monitor, and process various clinical parameters from an adult or neonate/infant populations in any type of clinical environment other than home use.
FDA Enforcement
Class II
·Terminated·Spacelabs Healthcare Inc·May 13, 2015