Medical Device Manufacturer · US , San Francisco , CA

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

1 submissions · 1 cleared · Since 2022

Total

Cleared

Denied

Wearlinq, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Francisco, US.

Last cleared in 2022. Active since 2022. Primary specialty: Cardiovascular.

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

Wearlinq, 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 - Wearlinq, Inc.

1 devices

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