Medical Device Manufacturer · US , Washington, Dc , DC

Nlt Spine, Ltd. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2011

Recent clearances: PROW FUSION-L, PROW FUSION-V, PROW FUSION

View 8 510(k) Devices ↓

Total

Cleared

Denied

Nlt Spine, Ltd. has 8 FDA 510(k) cleared medical devices. Based in Washington, Dc, US.

Historical record: 8 cleared submissions from 2011 to 2016. Primary specialty: Orthopedic.

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

510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.

Nlt Spine, Ltd. is one of 18387 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Nlt Spine, Ltd.

8 devices

1-8 of 8

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 16, 2026

Nlt Spine, Ltd. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Nlt Spine, Ltd.

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