Richmond Products, Inc.: FDA filings under this applicant name
FDA lists 15 510(k) clearances under the applicant name “Richmond Products, Inc.” (first 1987, latest 1988), across 12 product codes in 1 review panel. Median 510(k) review time under this name: 68 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 |
|---|---|---|---|
| HIT | Tester, Color Vision | 2 | 2 |
| HLP | Target, Fusion And Stereoscopic | 2 | 2 |
| HOX | Chart, Visual Acuity | 2 | 2 |
| HJD | Illuminator, Color Vision Plate | 1 | 1 |
| HKX | Tonometer, Ac-Powered | 1 | 1 |
| HOJ | Screen, Tangent, Target | 1 | 1 |
| HOO | Perimeter, Ac-Powered | 1 | 1 |
| HOQ | Grid, Amsler | 1 | 1 |
| HOR | Simulatan (Including Crossed Cylinder) | 1 | 1 |
| HPC | Set, Lens, Trial, Ophthalmic | 1 | 1 |
Plus 2 more product codes.
Review panels
- Ophthalmic (15)
Most recent Richmond Products, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K874252 | KREDA DISC | HOQ | 1988-01-27 | 100 |
| K874251 | WORTH 4 DOT TEST DISTANCE C/W MUSCLE LIGHT | HLP | 1988-01-11 | 84 |
| K874250 | THREE CHAR. TEST-CHILD & WORTH 4 DOT TEST NEARPT. | HLP | 1988-01-11 | 84 |
| K873907 | CONFIRMATION TESTS | HPC | 1987-12-29 | 95 |
| K873908 | H.R.R. PSEUDOISOCHROMATIC COLOR BLINDNESS TEST BK. | HIT | 1987-12-23 | 89 |
| K873916 | 'E' CUBE AND 'E' PAD | HOX | 1987-12-11 | 77 |
| K873914 | ANIMATED FIXATION TOYS (DISTANCE AND NEARPOINT) | HPL | 1987-12-11 | 77 |
| K873913 | COLOR BOOK ILLUMINATOR STAND | HJD | 1987-12-02 | 68 |
| K873911 | PSEUDO ISOCHROMATIC COLOR BLINDNESS TEST BOOK - 15 | HIT | 1987-12-02 | 68 |
| K873917 | TONOMETER TAPES | HKX | 1987-11-02 | 38 |
5 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Richmond 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.
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.
- The Richmond Light Co. (2 510(k)s)
- Richmond Diagnostics, Inc. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Richmond Products, Inc.?
FDA lists 15 510(k) clearances under the applicant name “Richmond Products, Inc.” (first 1987, latest 1988), across 12 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 Richmond Products, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Richmond Products, Inc. is 68 days.
Which FDA product codes appear under Richmond Products, Inc.?
The most frequent FDA product codes under this applicant name are HIT (Tester, Color Vision, 2); HLP (Target, Fusion And Stereoscopic, 2); HOX (Chart, Visual Acuity, 2).
Next steps
- See all 15 Richmond Products, Inc. clearances with predicates and recalls
- Run predicate analysis for product code HIT, Richmond 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 (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.