Cardon Rehabilitation Products, Inc.: FDA filings under this applicant name
FDA lists 16 510(k) clearances under the applicant name “Cardon Rehabilitation Products, Inc.” (first 1995, latest 1996), across 1 product code in 1 review panel. Median 510(k) review time under this name: 20 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 |
|---|---|---|---|
| INQ | Table, Powered | 16 | 16 |
Review panels
- Physical Medicine (16)
Most recent Cardon Rehabilitation Products, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K960336 | CARDON PHYSICAL THERAPY TABLE MODEL R27645 | INQ | 1996-02-13 | 20 |
| K960334 | CARDON PHYSICAL THERAPY TABLE MODEL R27116 | INQ | 1996-02-13 | 20 |
| K960332 | CARDON PHYSICAL THERAPY TABLE MODEL R28598 | INQ | 1996-02-13 | 20 |
| K951955 | CARDON PHYSICAL THERAPY TABLE MODEL:R40194 | INQ | 1995-06-22 | 57 |
| K951906 | CARDON PHYSICAL THERAPY TABLES MODELS R28591 & R28592 | INQ | 1995-06-15 | 52 |
| K951954 | CARDON PHYSICAL THERAPY TABLE MODEL R27108 | INQ | 1995-05-31 | 35 |
| K951953 | CARDON PHSICAL THERAPY TABLE MODEL R27630 | INQ | 1995-05-31 | 35 |
| K951952 | CARDON PHYSICAL THERAPY TABLE MODEL R27112 | INQ | 1995-05-31 | 35 |
| K950872 | CARDON PHYSICAL THERAPY TABLE MODEL: R27841 | INQ | 1995-05-25 | 86 |
| K950873 | CARDON PHYSICAL THERAPY TABLES MODELS: R27622 | INQ | 1995-04-10 | 41 |
6 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Cardon Rehabilitation Products, 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.
Frequently asked questions
How many FDA 510(k) clearances are listed under Cardon Rehabilitation Products, Inc.?
FDA lists 16 510(k) clearances under the applicant name “Cardon Rehabilitation Products, Inc.” (first 1995, latest 1996), 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 Cardon Rehabilitation Products, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Cardon Rehabilitation Products, Inc. is 20 days.
Which FDA product codes appear under Cardon Rehabilitation Products, Inc.?
The most frequent FDA product codes under this applicant name are INQ (Table, Powered, 16).
Next steps
- See all 16 Cardon Rehabilitation Products, Inc. clearances with predicates and recalls
- Run predicate analysis for product code INQ, Cardon Rehabilitation Products, 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, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.