Medical Device Manufacturer · FR , Marseille

Sopro - FDA 510(k) Cleared Devices

25 submissions · 25 cleared · Since 1997

Total

Cleared

Denied

Sopro has 25 FDA 510(k) cleared medical devices. Based in Marseille, FR.

Last cleared in 2023. Active since 1997. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Sopro Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Sopro

25 devices

1-12 of 25

Gastroenterology & Urology · 83d

General & Plastic Surgery · 190d

Cleared Jul 11, 2008

SOPRO 670 ARTHROSCOPIC PUMP

K080122 · HRX

Orthopedic · 176d

Cleared Dec 13, 2007

SOPRO MODEL 640 LAPAROSCOPIC INSUFFLATOR

K070783 · HIF

Obstetrics & Gynecology · 267d

Cleared Nov 16, 2007

SOPRO 225 DUAL HALOGEN LIGHT SOURCE

K072912 · GCJ

General & Plastic Surgery · 35d

Cleared Feb 20, 2007

SOPRO 162 CAMERA

K070102 · GCJ

General & Plastic Surgery · 41d

Cleared Sep 16, 2003

SOPRO 61D

K031593 · GCJ

General & Plastic Surgery · 118d

Cleared Jun 14, 2002

SOPRO LIGHT SOURCES AND ACCESSORIES

K020915 · GCJ

General & Plastic Surgery · 85d

Sopro - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Sopro

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