22 results · 23ms · Sources: EU EUDAMED, 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