Medical Device Manufacturer · US , Lewes , DE

Hinlab, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2023

Recent clearances: Pediarity™

Total

Cleared

Denied

Hinlab, Inc. has 1 FDA 510(k) cleared medical devices. Based in Lewes, US.

Last cleared in 2023. Active since 2023. Primary specialty: Anesthesiology.

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

Hinlab, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Hinlab, Inc.

1 devices

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