Medical Device Manufacturer · US , Great Neck , NY

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

1 submissions · 1 cleared · Since 2001

Total

Cleared

Denied

Nimble, Inc. has 1 FDA 510(k) cleared medical devices. Based in Great Neck, US.

Historical record: 1 cleared submissions from 2001 to 2001. Primary specialty: Physical Medicine.

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

Nimble, 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 - Nimble, Inc.

1 devices

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