Data / Medical devices / United States / Salt Logistics
Salt Logistics: FDA-registered device maker in Somerset, NJ, United States, 2 510(k) clearances
Salt Logistics is registered with the FDA (registration 3006195167) in Somerset, NJ, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated October 12, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006195167
- Address
- 645 Howard Avenue, Somerset, NJ, United States, 08873
- Owner or operator
- Chemtex USA, Inc. (10078515)
- Roles
- Complaint file establishment
- First device listed
- October 25, 2020
- Registered through
- 2026
- Brand names listed
- Aqua Naina Plus Sterile Saline Solution, Aqua Naina Sterile Saline Solution, Aqua Naina Sterile Saline Solution
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Soft Lens Products | LPN | 2 | Complaint file establishment | accessdata.fda.gov |
| Products, Contact Lens Care, Rigid Gas Permeable | MRC | 2 | Complaint file establishment | 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 |
|---|---|---|---|---|---|---|
| October 12, 2022 | K221263 | Aqua Naina Plus Sterile Saline Solution | LPN | Substantially Equivalent | Chemtex USA, Inc. | accessdata.fda.gov |
| May 26, 2020 | K193441 | Aqua Naina Sterile Saline Solution | LPN | Substantially Equivalent | Chemtex USA, 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 October 12, 2022. 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.