Kinetic Technology, Inc.: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Kinetic Technology, Inc.” (first 1988, latest 1992), across 1 product code in 1 review panel. Median 510(k) review time under this name: 118 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| LXM | Manipulator, Plunger-Like Joint | 5 | 5 |
Review panels
Most recent Kinetic Technology, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K922695 | KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5 | LXM | 1992-09-30 | 118 |
| K922694 | KINETIC TECHNOLOGY PRECISION ADUSTOR MODEL SHLCP-4 | LXM | 1992-09-30 | 118 |
| K922693 | KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1 | LXM | 1992-09-30 | 118 |
| K922692 | KINETIC TECHNOLOGY POCKET PRECISION ADJUSTOR | LXM | 1992-09-30 | 118 |
| K870910 | PRECISION SPINAL ADJUSTER MODEL 115 | LXM | 1988-04-26 | 418 |
Recalls
openFDA lists no recalls under a recalling firm named Kinetic Technology, Inc..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Kinetic Medical Products (63 510(k)s)
- Kinetic Concepts, Inc. (48 510(k)s)
- Kinetic Biomedical Services, Inc. (5 510(k)s)
- Kinetic Instruments, Inc. (2 510(k)s)
- Kinetic Surgical, LLC (2 510(k)s)
- Kinetic Innovative Seating System, LLC (1 510(k)s)
- Kinetic Rehabilitation Instruments, Inc. (1 510(k)s)
- Kinetic Resources, Inc. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Kinetic Technology, Inc.?
FDA lists 5 510(k) clearances under the applicant name “Kinetic Technology, Inc.” (first 1988, latest 1992), across 1 product code in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Kinetic Technology, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Kinetic Technology, Inc. is 118 days.
Which FDA product codes appear under Kinetic Technology, Inc.?
The most frequent FDA product codes under this applicant name are LXM (Manipulator, Plunger-Like Joint, 5).
Next steps
- See all 5 Kinetic Technology, Inc. clearances with predicates and recalls
- Run predicate analysis for product code LXM, Kinetic Technology, Inc.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.