Sota Precision Optics, Inc.
Orange, CA, US
SOTA PRECISION OPTICS, INC. appears in FDA device records in Orange, CA. FDA records list 3 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 3 510(k) clearances for Sota Precision Optics, Inc. between 2003 and 2011. The busiest year on record is 2003, with 1. The most recent is 2011, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2003 | 1 |
| 2006 | 1 |
| 2011 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K110886 | CLIO/CLIOSOFT | LLZ | Substantially Equivalent | |
| K061175 | CLARIS I310D INTRAORAL CAMERA SYSTEM & ACCESSORIES | EIA | Substantially Equivalent | |
| K032341 | INTRA ORAL CAMERA SYSTEM AND ACCESSORIES, MODEL CLARIS I310 | EIA | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3000190675 | 3000190675 | SOTA PRECISION OPTICS, INC. | 1073 N Batavia St Ste B, ORANGE, CA 92867 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain