Human Performance Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Human Performance Technologies, Inc. makes
Human Performance Technologies, Inc. manufactures real-time foot pressure measurement systems, such as the 2P-QDA, and gait/motion analysis systems, including the 2K-QDA. These devices are designed for clinical assessment of foot mechanics and lower-limb movement patterns, providing quantitative data for diagnostic and rehabilitative purposes.
The company’s products are regulated under FDA’s 510(k) pathway, with devices classified as Class I and Class II. The systems are listed in the FDA’s 510(k) database, reflecting their compliance with U.S. medical device regulations. The manufacturer is based in the United States.
Catalogue
2P-Qda Foot Pressure Systems Real Time Ref K882139
Regimes: 510(k) Registry: 510(k)2K-Qda Motion/Gait Analysis System Ref K880631
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Human Performance Technologies, Inc. have in the registry?
The registry currently lists 2 devices for Human Performance Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Human Performance Technologies, Inc.'s devices?
Among its 2 most recently registered devices, Human Performance Technologies, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Human Performance Technologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Human Performance Technologies, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Human Performance Technologies, Inc. in the registry?
The most recently registered devices listed for Human Performance Technologies, Inc. include 2P-QDA FOOT PRESSURE SYSTEMS REAL TIME and 2K-QDA MOTION/GAIT ANALYSIS SYSTEM.