Medical Device Manufacturer · US , Sacramento , CA

Hand Biomechanics Lab, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1994

Total

Cleared

Denied

Hand Biomechanics Lab, Inc. has 9 FDA 510(k) cleared medical devices. Based in Sacramento, US.

Latest FDA clearance: Oct 2025. Active since 1994. Primary specialty: Orthopedic.

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

FDA 510(k) cleared devices by Hand Biomechanics Lab, Inc.

9 devices

1-9 of 9

Cleared Oct 15, 2025

TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly

F3 FRACTURED FINGER FIXATOR, STERILE (MODEL: FCS 400) AND NON STERILE

K072432 · JEC

Orthopedic · 133d

Cleared Nov 05, 2003

WRISTJACK ORIF SYSTEM, WRISTJACK ORIF SYSTEM, NON-STERILE, MODELS CFD-347,...

K033112 · KTT

Orthopedic · 36d

Cleared Jun 10, 2003

WRISTJACK SYSTEM (REMANUFACTURED), STERILE AND NON-STERILE, MODELS...

AGEE-WRISTJACK FRACTURE REACTION SYSTEM (STERILE VERSION), MODEL CFD-147

K984442 · JEC

Orthopedic · 60d

Cleared Dec 22, 1994

AGEE-WRISTJACK PRE-DRILL KIT

K942906 · HTW

Orthopedic · 184d

Hand Biomechanics Lab, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Hand Biomechanics Lab, Inc.

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