22 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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WELCH ALLYN 11800 OPTHALMOSCOPE
FDA 510(k)
FDA Class 2
·Ophthalmic
Implant Prosthetics
FDA UDI
Preat Corporation·00842092102985·CAMLOG® Screw-Line-compatible 3.8mm Straight Mu...
Premier Elevator
FDA UDI
PREMIER DENTAL PRODUCTS COMPANY·00348783004137·ELEVATOR 39-CRYER
SCANLAN® Legacy Needle Holders
FDA UDI
SCANLAN INTERNATIONAL INC·00846159032864·Legacy Titanium Needle Holder, FH W/RAT 9" Reg BL
TI-MAX PROTRUSIO CAGE
FDA 510(k)
FDA Class 2
·Orthopedic
SPECIALTY 42 (HEFILCON A) HYDROPHILIC CONTACT LENS FOR DAILY WEAR, SPECIALTY T-42 TORIC (HEFILCON A) HYDROPHILIC CONTACT
FDA 510(k)
FDA Class 2
·Ophthalmic
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
CORONAL ROD BENDER - LEFT FOR
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HXW·February 28, 2013
CONCERTO CRT-D DR
FDA Adverse Event
Death
·MEDTRONIC MED REL, INC.·Product code NIK·March 1, 2011
MRI
FDA Adverse Event
Injury
·Product code LNH·February 22, 2008
ALARIS® PUMP MODULE ADMINISTRATION SET
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·February 19, 2016
APTIMA SARS-COV-2 ASSAY
FDA Adverse Event
Malfunction
·HOLOGIC INCORPORATED·Product code QJR·August 2, 2022
smiths medical PORTEX Tracheal Tube Exchange Guide, 10Ch x 70cm, REF 14-504-76
FDA Enforcement
Class II
·Ongoing·Smiths Medical ASD, Inc.·December 4, 2024