Data / Medical devices / Sweden / Peptonic Medical AB
Peptonic Medical AB: FDA-registered device maker in Bromma Stockholm, Sweden, 1 510(k) clearance
Peptonic Medical AB is registered with the FDA (registration 3019793660) in Bromma Stockholm, Sweden. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 10, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3019793660
- Address
- Gustavslundsvagen 143, Bromma Stockholm, Sweden, 16751
- Owner or operator
- Peptonic Medical AB (10082253)
- Roles
- Specification developer
- First device listed
- July 1, 2021
- Registered through
- 2026
- Brand names listed
- JUICY LIKE A PEACH, VagiVital AktivGel
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lubricant, Personal | NUC | 2 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| November 10, 2020 | K200098 | VagiVital Aktivgel | NUC | Substantially Equivalent | Peptonic Medical AB | accessdata.fda.gov |
Compare with other makers
Updated November 10, 2020. 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.