Medical Device Manufacturer · US , Draper , UT

Ortho Development Corp. - FDA 510(k) Cleared Devices

45 submissions · 43 cleared · Since 1996

Total

Cleared

Denied

Ortho Development Corp. has 43 FDA 510(k) cleared orthopedic devices. Based in Draper, US.

Latest FDA clearance: Dec 2025. Active since 1996.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Ortho Development Corp.

45 devices

1-12 of 45

Cleared Dec 19, 2025

Balanced Knee System TriMax Porous Femoral Components

Legend® Acetabular Shell

IBIS PEDICLE SCREW SYSTEM

K142146 · NKB

Orthopedic · 128d

Cleared Jun 20, 2014

ENCOMPASS 10/12 HIP STEM

K132697 · LPH

Orthopedic · 295d

Cleared Mar 11, 2014

OVATION TRIBUTE HIP STEM

K133386 · LPH

Orthopedic · 126d

Cleared Feb 18, 2014

KASM KNEE ARTICULATING SPACER MOLDS

K133449 · JWH

Orthopedic · 98d

Cleared Oct 16, 2013

OVATION 10/12 HIP STEM

K131022 · LPH

Orthopedic · 187d

Cleared Oct 11, 2013

BALANCED KNEE SYSTEM HIGH FLEX VITAMIN E PS TIBIAL INSERT AND PATELLA

K131337 · JWH

Orthopedic · 155d

Cleared Aug 20, 2013

PAGODA PEDICLE SCREW SYSTEM

K131785 · NKB

Orthopedic · 63d

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Ortho Development Corp. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Ortho Development Corp.

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