Data / Medical devices / United States / Pacific Ophthalmic Supply
Pacific Ophthalmic Supply: FDA-registered device maker in Belmont, CA, United States, 2 510(k) clearances
Pacific Ophthalmic Supply is registered with the FDA (registration 2952604) in Belmont, CA, United States. It lists 6 device types. The FDA files 2 510(k) clearances under its listings, the newest dated May 11, 2016. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2952604
- FEI number
- 3000210228
- Address
- 1924 Oak Knoll DR., Belmont, CA, United States, 94002
- Owner or operator
- PACIFIC OPHTHALMIC SUPPLY (9026364)
- Roles
- Repackager or relabeler
- First device listed
- July 23, 2010
- Registered through
- 2026
- Brand names listed
- Acuity Chart, Exophthalmometer, POS Lensmeter, POS Phoroptor, Slit Lamp, Trial Frame
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Biomicroscope, Slit-Lamp, Ac-Powered | HJO | 2 | Repackager or relabeler | accessdata.fda.gov |
| Chart, Visual Acuity | HOX | 1 | Repackager or relabeler | accessdata.fda.gov |
| Exophthalmometer | HLS | 1 | Repackager or relabeler | accessdata.fda.gov |
| Frame, Trial, Ophthalmic | HPA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Instrument, Measuring, Lens, Ac-Powered | HLM | 1 | Repackager or relabeler | accessdata.fda.gov |
| Refractor, Manual, Non-Powered, Including Phoropter | HKN | 1 | 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 |
|---|---|---|---|---|---|---|
| May 11, 2016 | K152429 | Slit Lamp Microscope | HJO | Substantially Equivalent | Shanghai Mediworks Precision Instruments Co. , Ltd. | accessdata.fda.gov |
| December 4, 2003 | K033190 | VISION-TECH YZ SLIT LAMP, MODEL 66 | HJO | Substantially Equivalent | Suzhou 66 Vision-Tech Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Chart, Visual Acuity
- All makers of Biomicroscope, Slit-Lamp, Ac-Powered
- All makers of Frame, Trial, Ophthalmic
- All makers of Instrument, Measuring, Lens, Ac-Powered
- All makers of Refractor, Manual, Non-Powered, Including Phoropter
- All makers of Exophthalmometer
Updated May 11, 2016. 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.