Data / Medical devices / United States / Altaire Pharmaceuticals, Inc.
Altaire Pharmaceuticals, Inc.: FDA-registered device maker in Aquebogue, NY, United States, 1 510(k) clearance
Altaire Pharmaceuticals, Inc. is registered with the FDA (registration 2335740) in Aquebogue, NY, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 25, 2007. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2335740
- FEI number
- 1000119582
- Address
- 311 West LN., Aquebogue, NY, United States, 11931
- Owner or operator
- ALTAIRE PHARMACEUTICALS, INC. (9047159)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- November 26, 2007
- Registered through
- 2026
- Brand names listed
- Altaire MPS#1 Multipurpose Contact, Clear Eyes CLR, Lobob C/D/S Solution, Lobob Cleaner, Lobob W/RW Drop
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Soft Lens Products | LPN | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Products, Contact Lens Care, Rigid Gas Permeable | MRC | 2 | Contract manufacturer, Manufacturer | 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 25, 2007 | K062332 | ALTAIRE MPS#1 MULTIPURPOSE CONTACT LENS SOLUTION | LPN | Substantially Equivalent | Altaire Pharmaceuticals, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Accessories, Soft Lens Products
- All makers of Products, Contact Lens Care, Rigid Gas Permeable
Updated April 25, 2007. 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.