Wieland Edelmetalle GmbH & Co.: FDA filings under this applicant name
FDA lists 14 510(k) clearances under the applicant name “Wieland Edelmetalle GmbH & Co.” (first 2000, latest 2002), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 70 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 |
|---|---|---|---|
| EJT | Alloy, Gold-Based Noble Metal | 10 | 10 |
| EJS | Alloy, Other Noble Metal | 3 | 3 |
| EIH | Powder, Porcelain | 1 | 1 |
Review panels
- Dental (14)
Most recent Wieland Edelmetalle GmbH & Co. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K020347 | AGC SPEZIALLEGIERUNG | EJT | 2002-04-24 | 79 |
| K012839 | AUROPAL, ORDER-NO.: 2101 | EJT | 2001-12-31 | 130 |
| K012841 | DUO PAL 6, ORDER-NO.: 2154 | EJS | 2001-11-20 | 89 |
| K012843 | PORTADUR P 2, MODEL #2031 | EJT | 2001-11-02 | 71 |
| K012835 | PORTA MAXIMUM, MODEL# 2066 | EJT | 2001-11-01 | 70 |
| K012834 | PORTA GEO TI MODEL #2004 | EJT | 2001-11-01 | 70 |
| K012831 | BIO PORTADUR, ORDER-NO.:2017 | EJT | 2001-11-01 | 70 |
| K012828 | PORTA SMK 82, MODEL 2032 | EJS | 2001-11-01 | 70 |
| K012827 | PORTA AURIUM, MODEL 2067 | EJT | 2001-11-01 | 70 |
| K012826 | BIOPORTA G, MODEL 2052 | EJT | 2001-11-01 | 70 |
4 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Wieland Edelmetalle GmbH & Co..
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.
- Wieland Dental + Technik GmbH & Co. KG (45 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Wieland Edelmetalle GmbH & Co.?
FDA lists 14 510(k) clearances under the applicant name “Wieland Edelmetalle GmbH & Co.” (first 2000, latest 2002), across 3 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 Wieland Edelmetalle GmbH & Co.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Wieland Edelmetalle GmbH & Co. is 70 days.
Which FDA product codes appear under Wieland Edelmetalle GmbH & Co.?
The most frequent FDA product codes under this applicant name are EJT (Alloy, Gold-Based Noble Metal, 10); EJS (Alloy, Other Noble Metal, 3); EIH (Powder, Porcelain, 1).
Next steps
- See all 14 Wieland Edelmetalle GmbH & Co. clearances with predicates and recalls
- Run predicate analysis for product code EJT, Wieland Edelmetalle GmbH & Co.'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.