Data / Medical devices / Italy / Hudi Pharma SRL
Hudi Pharma SRL: FDA-registered device maker in Milano, Italy, 1 510(k) clearance
Hudi Pharma SRL is registered with the FDA (registration 3015686320) in Milano, Italy. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 1, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015686320
- Address
- Piazza Giuseppe Grandi 19, Milano, Italy, 20129
- Owner or operator
- HUDI PHARMA SRL (10095795)
- Roles
- Specification developer
- First device listed
- April 30, 2026
- Registered through
- 2026
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 |
|---|---|---|---|---|---|---|
| April 1, 2026 | K260007 | Hyaluronic Acid Vaginal Suppository (HA 5 mg); Hyaluronic Acid Vaginal Suppository (HA 10 mg) | NUC | Substantially Equivalent | Hudi Pharma Srl | accessdata.fda.gov |
Compare with other makers
Updated April 1, 2026. 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.