This page includes the latest FDA filings for Limestone Technologies Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3005495199 | ||||||
| FEI Number | 3005495199 | ||||||
| Name | Kevin Walls | ||||||
| Owner & Operator | LIMESTONE TECHNOLOGIES INC. | ||||||
| Contact Address | 5076 E BATH RD -- BATH, ONTARIO CA-NOTA KOH 1GO CA | ||||||
| US Agent |
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| Importing Logistics Registration |
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| Registration Status | 1 | ||||||
| Initial Importer | N | ||||||
| Registration Expiration | 2020-04-25 | ||||||
| Registration Address | 33 Golden Eagle Lane Littleton, CO 80127 US | ||||||
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
LIMESTONE TECHNOLOGIES INC. | PREFTEST PROFESSIONAL SUITE | 2006-04-26 |
Kevin Walls [LIMESTONE TECHNOLOGIES INC.] | PREFTEST PROFESSIONAL SUITE | 2005-12-13 |
| NCAGE Code | L3433 | LIMESTONE TECHNOLOGIES INC |
| CAGE Code | L3433 | LIMESTONE TECHNOLOGIES INC |
| S.A.M. Registration | L3433 [200103286] | LIMESTONE TECHNOLOGIES INC |