Williams Gold Refining Co., Inc.: FDA filings under this applicant name
FDA lists 26 510(k) clearances under the applicant name “Williams Gold Refining Co., Inc.” (first 1976, latest 1986), across 6 product codes in 1 review panel. Median 510(k) review time under this name: 29 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 |
|---|---|---|---|
| EJS | Alloy, Other Noble Metal | 9 | 9 |
| EJT | Alloy, Gold-Based Noble Metal | 6 | 6 |
| EJH | Alloy, Metal, Base | 5 | 5 |
| EIH | Powder, Porcelain | 2 | 2 |
| EJP | Articulators | 1 | 1 |
Plus 1 more product codes.
Review panels
- Dental (23)
Most recent Williams Gold Refining Co., Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K855182 | ALLOY FOR METAL CROWN & BRIDGE YELLOW PD #46 & #65 | EJS | 1986-03-25 | 89 |
| K860439 | DW217 #18 CROWN/BRIDGE & DW218 #24 CERAMIC ALLOYS | EJS | 1986-03-20 | 44 |
| K854738 | SPARTAN SOLDER | EJH | 1986-03-06 | 101 |
| K852895 | CERAMIC ALLOY NO. DW 179 | EJH | 1985-10-21 | 104 |
| K852093 | ALLOY 7 | EJS | 1985-08-23 | 101 |
| K850699 | SPARTAN -ALLOY FOR PORCELAIN FUSED TO METAL | EJS | 1985-03-18 | 25 |
| K844395 | RENAISSANCE | EJT | 1985-01-09 | 57 |
| K844394 | RENAISSANCE BONDING AGENT | EJT | 1985-01-09 | 57 |
| K822419 | NEW CROWN AND BRIDGE ALLOY NO. DW196 | EJS | 1982-08-30 | 19 |
| K821510 | A THENIUM | EJS | 1982-06-09 | 20 |
16 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Williams Gold Refining Co., 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.
- Williams Medical Co. (5 510(k)s)
- Williams Manufacturing Co. (4 510(k)s)
- Williams Sound, LLC (4 510(k)s)
- Williams Dental Co., Inc. (2 510(k)s)
- Williams Healthcare Systems, LLC (2 510(k)s)
- Williams Specialty Products, Inc. (2 510(k)s)
- Williams Airway Intubator (1 510(k)s)
- Williams & Connolly (1 510(k)s)
- Williams Importing Company, Inc. (1 510(k)s)
- Williams, the J.B. Co., Inc. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Williams Gold Refining Co., Inc.?
FDA lists 26 510(k) clearances under the applicant name “Williams Gold Refining Co., Inc.” (first 1976, latest 1986), 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 Williams Gold Refining Co., Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Williams Gold Refining Co., Inc. is 29 days.
Which FDA product codes appear under Williams Gold Refining Co., Inc.?
The most frequent FDA product codes under this applicant name are EJS (Alloy, Other Noble Metal, 9); EJT (Alloy, Gold-Based Noble Metal, 6); EJH (Alloy, Metal, Base, 5).
Next steps
- See all 26 Williams Gold Refining Co., Inc. clearances with predicates and recalls
- Run predicate analysis for product code EJS, Williams Gold Refining Co., 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.