Hosmer Dorrance Corp.: FDA filings under this applicant name
FDA lists 9 510(k) clearances under the applicant name “Hosmer Dorrance Corp.” (first 1977, latest 1982), across 6 product codes in 1 review panel. Median 510(k) review time under this name: 14 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 |
|---|---|---|---|
| IQI | Orthosis, Limb Brace | 3 | 3 |
| ION | Exerciser, Non-Measuring | 2 | 2 |
| IQX | Hook, External Limb Component, Mechanical | 1 | 1 |
| IRE | Joint, Elbow, External Limb Component, Powered | 1 | 1 |
| ITQ | Joint, Knee, External Brace | 1 | 1 |
| ITS | Joint, Hip, External Brace | 1 | 1 |
Review panels
Most recent Hosmer Dorrance Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K822632 | ELBOW PROSTHESIS | IRE | 1982-09-14 | 14 |
| K821704 | FRACTURE BRACING | IQI | 1982-06-24 | 22 |
| K801788 | HUMEROUS FRACTURE BRACE, ULNA FRACTURE | IQI | 1980-08-07 | 9 |
| K780892 | FRACTURE BRACING | ITQ | 1978-06-13 | 13 |
| K780891 | POST-OPERATIVE HIP ORTHOSIS | ITS | 1978-06-13 | 13 |
| K780890 | CAPP TERMINAL DEVICE | IQX | 1978-06-13 | 13 |
| K761314 | FLEXION-BRAKING KNEE-SHIN ASSEMBLY | ION | 1977-01-10 | 18 |
| K761313 | 4-BAR KNEE-SHIN SET-UP | ION | 1977-01-10 | 28 |
| K761312 | ORTHOTIC BRACING | IQI | 1977-01-10 | 18 |
Recalls
openFDA lists no recalls under a recalling firm named Hosmer Dorrance Corp..
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 Hosmer Dorrance Corp.?
FDA lists 9 510(k) clearances under the applicant name “Hosmer Dorrance Corp.” (first 1977, latest 1982), across 6 product codes 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 Hosmer Dorrance Corp.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Hosmer Dorrance Corp. is 14 days.
Which FDA product codes appear under Hosmer Dorrance Corp.?
The most frequent FDA product codes under this applicant name are IQI (Orthosis, Limb Brace, 3); ION (Exerciser, Non-Measuring, 2); IQX (Hook, External Limb Component, Mechanical, 1).
Next steps
- See all 9 Hosmer Dorrance Corp. clearances with predicates and recalls
- Run predicate analysis for product code IQI, Hosmer Dorrance Corp.'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.