Medical Device Manufacturer · TH , Muang Nonthaburi

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

3 submissions · 3 cleared · Since 2021
3
Total
3
Cleared
0
Denied

Meticuly Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Muang Nonthaburi, TH.

Latest FDA clearance: Jan 2026. Active since 2021. Primary specialty: Neurology.

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

510(k) submissions have been managed by Mdr Solutions Co., Ltd. as regulatory consultant.

FDA 510(k) Regulatory Record - Meticuly Co., Ltd.
3 devices
1-3 of 3
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