Tannhut: FDA filings under this applicant name
FDA lists 7 510(k) clearances under the applicant name “Tannhut” (first 1981, latest 1985), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 28 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 |
|---|---|---|---|
| FTC | Light, Ultraviolet, Dermatological | 5 | 5 |
| LEJ | Booth, Sun Tan | 1 | 1 |
Plus 1 more product codes.
Review panels
Most recent Tannhut 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K851859 | FACIAL/UPPER BODY UNIT | FTC | 1985-05-14 | 18 |
| K851858 | FOLD AWAY HUT | FTC | 1985-05-14 | 18 |
| K851255 | SUN BEDS | FTC | 1985-04-18 | 21 |
| K840137 | SILGMANN SOLARIUM S-TYPE 1218 COMBO | FTC | 1984-04-23 | 104 |
| K837283 | UNKNOWN | — | 1983-04-15 | 35 |
| K812579 | SUNTANNING HOME UNIT | FTC | 1981-10-08 | 28 |
| K802756 | SEMI-OVAL MODULAR SUNTANNING BOOTH | LEJ | 1981-01-22 | 78 |
Recalls
openFDA lists no recalls under a recalling firm named Tannhut.
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 Tannhut?
FDA lists 7 510(k) clearances under the applicant name “Tannhut” (first 1981, latest 1985), 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 Tannhut?
The median time from FDA receipt to decision across 510(k)s cleared under the name Tannhut is 28 days.
Which FDA product codes appear under Tannhut?
The most frequent FDA product codes under this applicant name are FTC (Light, Ultraviolet, Dermatological, 5); LEJ (Booth, Sun Tan, 1).
Next steps
- See all 7 Tannhut clearances with predicates and recalls
- Run predicate analysis for product code FTC, Tannhut'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.