Data / Medical devices / Germany / DC Altfeld - Procter & Gamble
DC Altfeld - Procter & Gamble: FDA-registered device maker in Marktheidenfeld Hesse, Germany, 5 510(k) clearances
DC Altfeld - Procter & Gamble is registered with the FDA (registration 3010912900) in Marktheidenfeld Hesse, Germany. It lists 3 device types. The FDA files 5 510(k) clearances under its listings, the newest dated March 18, 2019. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3010912900
- Address
- Max Braun Strasse 12, Marktheidenfeld Hesse, Germany, D-97828
- Owner or operator
- Procter & Gamble (9915005)
- Roles
- Exporter to the US
- First device listed
- December 22, 2015
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Light Based Over-The-Counter Hair Removal | OHT | 2 | Exporter to the US | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Exporter to the US | accessdata.fda.gov |
| Powered Light Based Non-Laser Surgical Instrument With Thermal Effect | ONF | 2 | Exporter to the US | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 18, 2019 | K190366 | BRAUN Silk Expert Pro 3 | OHT | Substantially Equivalent | Cyden Limited | accessdata.fda.gov |
| March 18, 2019 | K190354 | BRAUN Silk.expert Pro 5 | OHT | Substantially Equivalent | Cyden Limited | accessdata.fda.gov |
| May 8, 2017 | K170734 | Venus Silk.expert | GEX | Substantially Equivalent | Cyden Limited | accessdata.fda.gov |
| November 16, 2016 | K162231 | iPulse SmoothSkin Gold Hair Removal Device, Venus Silk.expert | OHT | Substantially Equivalent | Cyden Limited | accessdata.fda.gov |
| June 18, 2015 | K143003 | iPulse Smooth Skin Gold Hair Removal System | OHT | Substantially Equivalent | Ipulse Limited | accessdata.fda.gov |
Compare with other makers
- All makers of Light Based Over-The-Counter Hair Removal
- All makers of Powered Laser Surgical Instrument
- All makers of Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
Updated March 18, 2019. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.