10 results · 19ms · Sources: EU EUDAMED, US FDA

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CHEMONUCLEOLYSIS TABLE EXTENSION

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

Easter S.L Bracket, .022 Roth, LR2

FDA UDI
Astar Orthodontics Inc.·06941673516181·

LEDEX

FDA 510(k)
FDA Class 2 ·Dental

ATAC HEMOGLOBIN A1C REAGENT KIT

FDA 510(k)
FDA Class 2 ·Hematology

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·May 23, 2014

LRG TAP PRI MOD NCK 0DEG 30MM

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS CORK·Product code MEH·November 2, 2012

EPIC PLUS DR

FDA Adverse Event
Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 10, 2010

(1) Vanguard Knee System PS Open Box Femoral; Right; 60 mm. Intended for knee joint replacement prostheses. Item Number: 183104 (2) Vanguard Knee System PS Open Box Femoral; Right; 62.5 mm Item Number: 183106 (3) Vanguard Knee System PS Open Box Femoral; Right; 65 mm Item Number: 183108 (4) Vanguard Knee System PS Open Box Femoral; Right; 67.5 mm Item Number: 183110 (5) Vanguard Knee System PS Open Box Femoral; Right; 70 mm Item Number: 183112

FDA Enforcement
Class II ·Ongoing·Biomet, Inc.·February 8, 2023

(1) Vanguard Knee System PS Open Box Femoral; Right; 60 mm. Intended for knee joint replacement prostheses. Item Number: 183104 (2) Vanguard Knee System PS Open Box Femoral; Right; 62.5 mm Item Number: 183106 (3) Vanguard Knee System PS Open Box Femoral; Right; 65 mm Item Number: 183108 (4) Vanguard Knee System PS Open Box Femoral; Right; 67.5 mm Item Number: 183110 (5) Vanguard Knee System PS Open Box Femoral; Right; 70 mm Item Number: 183112

FDA Recall
Open, Classified ·Biomet, Inc.·Product code JWH·December 29, 2022

Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

FDA Enforcement
Class II ·Terminated·St Jude Medical Inc.·July 4, 2018