This page includes the latest FDA filings for Clarvista Medical. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3011665481 |
| FEI Number | 3011665481 |
| Name | CLARVISTA MEDICAL |
| Owner & Operator | Alcon Laboratories, Inc. |
| Contact Address | 6201 SOUTH FREEWAY Fort Worth TX 76134 US |
| Official Correspondent |
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| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 20511 Lake Forest Drive Lake Forest, CA 92630 US |
| Establishment Type | Manufacture Device in the United States for Export Only |
Device Company | Device | Date |
|---|---|---|
CLARVISTA MEDICAL [Alcon Laboratories, Inc.] | Intraocular Lens | 2018-11-06 |