13 results · 21ms · Sources: EU EUDAMED, US FDA

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OXYGEN CONCENTRATOR

FDA 510(k)
FDA Class 2 ·Anesthesiology

Spud

FDA UDI
KATENA PRODUCTS, INC.·00841668101223·ELLIS FOREIGN BODY SPUD

Instrument Case

FDA UDI
KATENA PRODUCTS, INC.·00841668111000·INSTRUMENT CADDY SMALL

Arthrex®

FDA UDI
ARTHREX, INC.·00888867415355·SECONDARY GLENOID IMPACTOR

Pulmoguard

FDA UDI
S D I DIAGNOSTICS INC·B279S297924100·Pulmonary Function Test Filter

IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR/MODEL: WL-2206, WELL IF, LIFE IF AND THE CUSTOMER PRIVATE BRAND

FDA 510(k)
FDA Class 2 ·Neurology

DSL SEX HORMONE BINDING GLOBULIN (SHBG) (DSL 6300)

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

PROGRASP (TM) FORCEPS

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·January 22, 2013

SPRINT QUATTRO

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 14, 2010

TENDRIL ST

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014

M2A-MAGNUM CUP

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 22, 2018

2.7MM/3.5MM VA-LCP X-ARTICLR PROXIMAL ULNA PL 8H/RT/157MM

FDA Adverse Event
Injury ·WRIGHTS LANE : SYNTHES USA PRODUCTS LLC·Product code HRS·December 29, 2017

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FDA Enforcement
Class II ·Terminated·Zimmer Biomet, Inc.·December 4, 2019