Data / Medical devices / Lebanon / Optical Supplies Company Sarl
Optical Supplies Company Sarl: FDA-registered device maker in Hazmieh, Beabda Mount Beyrouth, Lebanon, 1 510(k) clearance
Optical Supplies Company Sarl is registered with the FDA (registration 3008325767) in Hazmieh, Beabda Mount Beyrouth, Lebanon. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 16, 2002. 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
- 3008325767
- Address
- Saed Frayha, Hazmieh, Beabda Mount Beyrouth, Lebanon, none
- Owner or operator
- Optical Supplies Company SARL (10058017)
- Roles
- Exporter to the US
- First device listed
- June 26, 2018
- Registered through
- 2026
- Brand names listed
- Bella Contact Lenses
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lenses, Soft Contact, Daily Wear | LPL | 2 | Exporter to the US | 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 16, 2002 | K020608 | HD/HDT, (POLYMACON) SOFT CONTACT LENS FOR DAILY WEAR (CLEAR AND TINTED, FULLY CAST-MOLDED LENS) | LPL | Substantially Equivalent | Poly Vue Technolgies, Inc. | accessdata.fda.gov |
Compare with other makers
Updated May 16, 2002. 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.