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Hand Biomechanics Lab, Inc.

FDA 510(k) & PMA Approved Devices — 9 products

Total Devices9

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K252020	TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly	HRX	2025-10-15	View
510(k)	K222490	HBL Blade Assembly	HRX	2022-11-14	View
510(k)	K181192	PIP Fix	JEC	2018-10-22	View
510(k)	K072432	F3 FRACTURED FINGER FIXATOR, STERILE (MODEL: FCS 400) AND NON STERILE	JEC	2008-01-09	View
510(k)	K033112	WRISTJACK ORIF SYSTEM, WRISTJACK ORIF SYSTEM, NON-STERILE, MODELS CFD-347, CFD-347-NS	KTT	2003-11-05	View
510(k)	K030519	WRISTJACK SYSTEM (REMANUFACTURED), STERILE AND NON-STERILE, MODELS CFD-147-RS, CFD-247-RNS	JEC	2003-06-10	View
510(k)	K992970	DIGIT WIDGET	JDW	1999-11-08	View
510(k)	K984442	AGEE-WRISTJACK FRACTURE REACTION SYSTEM (STERILE VERSION), MODEL CFD-147	JEC	1999-02-12	View
510(k)	K942906	AGEE-WRISTJACK PRE-DRILL KIT	HTW	1994-12-22	View

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