Medical Device Manufacturer · US , Washington , DC

NormaTec Industries, LP - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2012

Total

Cleared

Denied

NormaTec Industries, LP has 9 FDA 510(k) cleared medical devices. Based in Washington, US.

Latest FDA clearance: Sep 2025. Active since 2012. Primary specialty: Physical Medicine.

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

FDA 510(k) cleared devices by NormaTec Industries, LP

9 devices

1-9 of 9

Cleared Sep 18, 2025

Normatec Elite Hip

K251905 · IRP

Physical Medicine · 90d

Cleared Mar 21, 2024

Normatec Elite

K240122 · IRP

Physical Medicine · 65d

Cleared Jul 14, 2022

Normatec Go

K221666 · IRP

Physical Medicine · 36d

Cleared Feb 25, 2022

Normatec 3

K220217 · IRP

Physical Medicine · 30d

Cleared Dec 27, 2018

Pulse 2.0, Pulse Pro 2.0

K183169 · IRP

Physical Medicine · 41d

Cleared Dec 21, 2018

Pulse Rx 2.0, Pulse Pro Rx 2.0

K183328 · JOW

Cardiovascular · 21d

Cleared Jun 15, 2016

NormaTec PCD-T and PCD-B

K161346 · JOW

Cardiovascular · 30d

Cleared Apr 13, 2016

NormaTec Pulse and NormaTec Pulse Pro

K160608 · IRP

Physical Medicine · 41d

Cleared Jan 04, 2012

NORMATEC MVP

K112890 · IRP

Physical Medicine · 96d

NormaTec Industries, LP - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by NormaTec Industries, LP

Filters