Data / Medical devices / Italy / Alliance Pharma SRL
Alliance Pharma SRL: FDA-registered device maker in Milan Lombardy, Italy, 3 510(k) clearances
Alliance Pharma SRL is registered with the FDA (registration 3013576473) in Milan Lombardy, Italy. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated January 13, 2005. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013576473
- Address
- Viale Restelli 5, Milan Lombardy, Italy, 20124
- Owner or operator
- Alliance Pharma SRL (10052705)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- January 3, 2017
- Registered through
- 2026
- Brand names listed
- Aloclair Oral Gel, Canker-X Mouth Sore Gel, Aloclair Oral Rinse, Canker-X Rincinol Mouth Sore Rinse, Aloclair Oral Spray, Canker-X Mouth Sore Spray
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Oral Wound Dressing | OLR | U | Complaint file establishment, 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 |
|---|---|---|---|---|---|---|
| January 13, 2005 | K042722 | ALOCLAIR ORAL SPRAY | OLR | Substantially Equivalent | Sinclair Pharmaceuticals, Ltd. | accessdata.fda.gov |
| June 21, 2004 | K040950 | ALOCLAIR ORAL GEL | OLR | Substantially Equivalent | Sinclair Pharmaceuticals, Ltd. | accessdata.fda.gov |
| November 25, 2002 | K023155 | ALOCLAIR ORAL RINSE | OLR | Substantially Equivalent | Sinclair Pharmaceuticals, Ltd. | accessdata.fda.gov |
Compare with other makers
Updated January 13, 2005. 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.