Hand Biomechanics Lab, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hand Biomechanics Lab, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly, HBL Blade Assembly, PIP Fix
9
Total
9
Cleared
0
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) Regulatory Record - Hand Biomechanics Lab, Inc.
9 devices
Cleared
Oct 15, 2025
TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly
Orthopedic
107d
Cleared
Nov 14, 2022
HBL Blade Assembly
Orthopedic
89d
Cleared
Oct 22, 2018
PIP Fix
Orthopedic
171d
Cleared
Jan 09, 2008
F3 FRACTURED FINGER FIXATOR, STERILE (MODEL: FCS 400) AND NON STERILE
Orthopedic
133d
Cleared
Nov 05, 2003
WRISTJACK ORIF SYSTEM, WRISTJACK ORIF SYSTEM, NON-STERILE, MODELS CFD-347,...
Orthopedic
36d
Cleared
Jun 10, 2003
WRISTJACK SYSTEM (REMANUFACTURED), STERILE AND NON-STERILE, MODELS...
Orthopedic
111d
Cleared
Nov 08, 1999
DIGIT WIDGET
Orthopedic
66d
Cleared
Feb 12, 1999
AGEE-WRISTJACK FRACTURE REACTION SYSTEM (STERILE VERSION), MODEL CFD-147
Orthopedic
60d
Cleared
Dec 22, 1994
AGEE-WRISTJACK PRE-DRILL KIT
Orthopedic
184d