Medical Device Manufacturer · US , Brookeville , MD

Ito Co., Ltd. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1999

Recent clearances: D function, US-101L, US-103S, MODEL ES-130

Total

Cleared

Denied

Ito Co., Ltd. has 8 FDA 510(k) cleared medical devices. Based in Brookeville, US.

Last cleared in 2021. Active since 1999. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Ito Co., Ltd. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Tuv Sud America, Inc. as regulatory consultant.

Ito Co., Ltd. is one of 16429 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ito Co., Ltd.

8 devices

1-8 of 8

Physical Medicine · 56d

Physical Medicine · 116d

Cleared Oct 09, 2003

US-100 PORTABLE ULTRASOUND THERAPY UNIT

K032793 · IMI

Physical Medicine · 30d

Cleared Jan 28, 2003

SW-180 SHORTWAVE THERAPY UNIT

K022846 · IMJ

Physical Medicine · 154d

Cleared Oct 20, 1999

TRIO 300

K990787 · IPF

Physical Medicine · 224d

Cleared Sep 01, 1999

TM-300 TRACTION SYSTEM

K992545 · ITH

Physical Medicine · 33d

Ito Co., Ltd. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Ito Co., Ltd.

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