Data / Medical devices / United States / Anschel Technology Inc.
Anschel Technology Inc.: FDA-registered device maker in Rocky Point, NY, United States, 1 510(k) clearance
Anschel Technology Inc. is registered with the FDA (registration 3010120146) in Rocky Point, NY, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 6, 2012. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010120146
- Address
- 1 Wildwood Rd, Rocky Point, NY, United States, 11778
- Owner or operator
- Anschel Technology Inc. (10043846)
- Roles
- Specification developer
- First device listed
- March 28, 2013
- Registered through
- 2026
- Brand names listed
- SightSaver
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Photic, Evoked Response | GWE | 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 |
|---|---|---|---|---|---|---|
| June 6, 2012 | K113785 | ADHERENT VISUAL STIMULATOR GOGGLES | GWE | Substantially Equivalent | Anschel Technology, Inc. | accessdata.fda.gov |
Compare with other makers
Updated June 6, 2012. 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.