Data / Medical devices / United States / Optical Connection Technology Inc.
Optical Connection Technology Inc.: FDA-registered device maker in San Diego, CA, United States, 10 510(k) clearances
Optical Connection Technology Inc. is registered with the FDA (registration 2024119) in San Diego, CA, United States. It lists 2 device types. The FDA files 10 510(k) clearances under its listings, the newest dated September 10, 2025. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 2024119
- Address
- 15980 Bernardo Center Dr, San Diego, CA, United States, 92127
- Owner or operator
- Optical Connection Technology Inc. (10050424)
- Roles
- Complaint file establishment, Repackager or relabeler
- First device listed
- November 16, 2015
- Registered through
- 2026
- Brand names listed
- BioCurve Spherical Silicone Hydrogel, Definition, IDEAL SiHy Contact Lenses
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lens, Contact, (Disposable) | MVN | 2 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Lenses, Soft Contact, Daily Wear | LPL | 2 | Complaint file establishment, Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| September 10, 2025 | K251573 | VizionFocus (somofilcon A) Silicone Hydrogel Soft (hydrophilic) Contact Lens | LPL | Substantially Equivalent | Vizionfocus, Inc. | accessdata.fda.gov |
| December 17, 2024 | K242413 | VizionFocus (mififilcon A) Silicone Hydrogel Soft (hydrophilic) Daily Disposable Contact Lens; VizionFocus Color (mififilcon A) Silicone Hydrogel Soft (hydrophilic) Daily Disposable Contact Lens | LPL | Substantially Equivalent | Vizionfocus, Inc. | accessdata.fda.gov |
| January 18, 2022 | K213216 | Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens | LPL | Substantially Equivalent | Unicon Optical Co., Ltd. | accessdata.fda.gov |
| September 17, 2019 | K191929 | UNICON Hydrogel (Hioxifilcon A) Soft (Hydrophilic) Contact Lens | LPL | Substantially Equivalent | Unicon Optical Co., Ltd. | accessdata.fda.gov |
| October 12, 2018 | K182247 | ILICON (ocufilcon D) Soft (Hydrophilic) Daily Wear Contact Lenses (Tinted, Color) | LPL | Substantially Equivalent | Vizionfocus, Inc. | accessdata.fda.gov |
| June 22, 2015 | K141348 | VISCO SOFT CONTACT LENS | LPL | Substantially Equivalent | Visco Vision, Inc. | accessdata.fda.gov |
| October 26, 2012 | K121201 | SAVIE-AQUA 55UV (METHAFILCON A) TINNTED BLUE SOFT (HYDROPHILIC) CONTACT LENS | LPL | Substantially Equivalent | St. shine Optical Co., Ltd. | accessdata.fda.gov |
| March 11, 2010 | K092852 | SAVIEW 58 UV; TORIC & MULTIFOCAL (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR | LPL | Substantially Equivalent | St. shine Optical Co., Ltd. | accessdata.fda.gov |
| September 3, 2009 | K083288 | DISCON PLUS (ETAFILCON A) CONTACT LENS VISIBILITY TINT WITH UV BLOCKER | LPL | Substantially Equivalent | Innova Vision, Inc. | accessdata.fda.gov |
| August 16, 2005 | K051095 | 55 UV (METHAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR | LPL | Substantially Equivalent | Optical Connection, Inc. | accessdata.fda.gov |
Compare with other makers
Updated September 10, 2025. 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.