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UNKNOWN HIP FEMORAL HEAD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·October 1, 2019

UNKNOWN HIP FEMORAL STEM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·October 1, 2019

Irrigator, Sinus

FDA classification
FDA Class 1 ·Irrigator, Sinus

CLAV FRAC PLT,CENTRAL THIRD,LFT,SS

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HRS·November 6, 2019

Mallinckrodt Dar S.r.l.

FDA registration
Mallinckrodt Dar S.r.l.·10 products·🇮🇹 Italy

Mallinckrodt Dar S.r.l.

FDA registration
Mallinckrodt Dar S.r.l.·4 products·🇮🇹 Italy

INSTRUMENT CASE, UNIVERS VAULTLOCK GLEN

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code MDM·May 1, 2024

PEGGED GLENOID TRIL & DRILL GUIDE CADDY

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code MDM·June 17, 2024

CLAV FRAC PLT,CENTRAL THIRD,RT,SS

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HRS·June 25, 2019

JSL CAR ACCESSORIES CO., LTD.

FDA registration
JSL CAR ACCESSORIES CO., LTD.·17 products·🇨🇳 China

THERMAGE FLX

FDA UDI
SOLTA MEDICAL·00816995027041·Thermage FLX System, Refurbished

UNIVERSAL GLENOID - BASEPLATE MEDIUM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·October 30, 2019

UNIVERS REVERS GLENO 42 +4 LAT

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·October 30, 2019

ANGLED REAMER SLEEVE, 10°

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·November 17, 2023

ANGLED REAMER SLEEVE, 10°

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·November 22, 2023

LightBeam

FDA UDI
EAR TECHNOLOGY CORPORATION·00810323001864·50 Pieces of Lighted Large Spoon Curette

LightBeam

FDA UDI
EAR TECHNOLOGY CORPORATION·00810323001871·50 pieces of Lighted Small Circle Loop Curette

TransEar

FDA UDI
EAR TECHNOLOGY CORPORATION·00810323003806·bone conduction hearing aid -

LightBeam

FDA UDI
EAR TECHNOLOGY CORPORATION·00810323001826·50 pieces of Lighted Small Spoon Curette

LightBeam

FDA UDI
EAR TECHNOLOGY CORPORATION·00810323005718·Replacement charging base, includes cable