Orthoconcept, Inc.: FDA filings under this applicant name
FDA lists 8 510(k) clearances under the applicant name “Orthoconcept, Inc.” (first 1987, latest 1994), across 2 product codes in 2 review panels. Median 510(k) review time under this name: 60 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 |
|---|---|---|---|
| HRX | Arthroscope | 6 | 6 |
| FDC | Resectoscope, Working Element | 2 | 2 |
Review panels
Most recent Orthoconcept, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K925160 | ARTHRO FMS 4 | HRX | 1994-02-17 | 492 |
| K910164 | ORTHOCONCEPT ARTHROSCOPIC PUMP | HRX | 1991-03-27 | 71 |
| K905785 | ARTHRO-FMS-3/IRRIGATION SETS (VARIOUS) | HRX | 1991-03-26 | 97 |
| K896196 | ARTHROSCOPY DISP. & REUSABLE SHAVER BLADES, RECHAR | HRX | 1989-12-01 | 37 |
| K895643 | MODIFIED UROPUMP* FLUID MANAGEMENT SYSTEM | FDC | 1989-10-17 | 50 |
| K894363 | UROPUMP* FLUID MANAGEMENT SYSTEM | FDC | 1989-08-11 | 28 |
| K882469 | CORDEX SHAVER, BLADES, RECHARGER AND BATTERIES | HRX | 1988-12-01 | 169 |
| K872270 | ORTHOCONCEPT ARTHROSCOPIC PUMP ORTHOPUMP | HRX | 1987-07-21 | 39 |
Recalls
openFDA lists no recalls under a recalling firm named Orthoconcept, 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 Orthoconcept, Inc.?
FDA lists 8 510(k) clearances under the applicant name “Orthoconcept, Inc.” (first 1987, latest 1994), across 2 product codes in 2 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Orthoconcept, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Orthoconcept, Inc. is 60 days.
Which FDA product codes appear under Orthoconcept, Inc.?
The most frequent FDA product codes under this applicant name are HRX (Arthroscope, 6); FDC (Resectoscope, Working Element, 2).
Next steps
- See all 8 Orthoconcept, Inc. clearances with predicates and recalls
- Run predicate analysis for product code HRX, Orthoconcept, 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.