Data / Medical devices / United States / Kontur Kontact Lens Co., Inc.
Kontur Kontact Lens Co., Inc.: FDA-registered device maker in Hercules, CA, United States, 1 PMA approval
Kontur Kontact Lens Co., Inc. is registered with the FDA (registration 2919245) in Hercules, CA, United States. It lists 2 device types. The FDA files 1 PMA approval under its listings, the newest dated January 31, 1986. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 2919245
- Address
- 642 Alfred Nobel DR., Hercules, CA, United States, 94547
- Owner or operator
- KONTUR KONTACT LENS CO., INC. (2919245)
- Roles
- Manufacturer
- First device listed
- December 17, 2007
- Registered through
- 2027
- Brand names listed
- Kontur 55 Sphere, Kontur 55 Toric, Kontur Precision Sphere
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lenses, Soft Contact, Daily Wear | LPL | 2 | Manufacturer | accessdata.fda.gov |
| Lenses, Soft Contact, Extended Wear | LPM | 3 | Manufacturer | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| January 31, 1986 | P850078 | KONTUR 55 EW | LPM | 10 | January 3, 1990 | accessdata.fda.gov |
Compare with other makers
Updated January 3, 1990. 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.