Kinetic Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Kinetic Technology, Inc. makes
Kinetic Technology, Inc. manufactures Class I precision spinal adjusters, including handheld and pocket-sized models designed for spinal manipulation. These devices are intended for use in chiropractic and orthopedic settings to apply controlled adjustments to the spine, such as the Precision Spinal Adjuster Model 115 and various SHLCP-series models.
The company’s portfolio is regulated under the FDA’s 510(k) pathway as Class I devices, indicating they are subject to general controls and pre-market notification requirements. These devices are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Precision Spinal Adjuster Model 115 Ref K870910
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Kinetic Technology Pocket Precision Adjustor Ref K922692
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kinetic Technology, Inc. have in the registry?
The registry currently lists 5 devices for Kinetic Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kinetic Technology, Inc.'s devices?
Among its 5 most recently registered devices, Kinetic Technology, Inc. has devices listed in FDA 510(k) (5 devices).
What are the newest devices from Kinetic Technology, Inc. in the registry?
The most recently registered devices listed for Kinetic Technology, Inc. include PRECISION SPINAL ADJUSTER MODEL 115, KINETIC TECHNOLOGY PRECISION ADUSTOR MODEL SHLCP-4, KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5 and KINETIC TECHNOLOGY POCKET PRECISION ADJUSTOR.