This page includes the latest FDA filings for Lameditech Co L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Registration Number | 3014384451 |
FEI Number | 3014384451 |
Name | Andrea Geffon |
Owner & Operator | LAMEDITECH Co., Ltd. |
Contact Address | #1002, ACE High End Tower 6th, Beotkkot- Seoul KR-11 Seoul Teugbyeolsi 08513 KR |
Official Correspondent |
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US Agent |
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Registration Status | 1 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | 38 industrial way east, suite 1 Eatontown, NJ 07724 US |
Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
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Lameditech Co., Ltd. | HandyRay-Lite | 2021-06-18 |
Lameditech Co., Ltd. | HandyRay-Pro | 2020-07-09 |
Andrea Geffon [LAMEDITECH Co., Ltd.] | HandyRay | 2018-03-29 |
Lameditech Co., Ltd. | LMT-3000 | 2018-03-07 |
NCAGE Code | 767FF | LAMEDITECH CO., LTD. |
CAGE Code | 767FF | LAMEDITECH CO., LTD. |
S.A.M. Registration | 767FF [689004243] | LAMEDITECH CO., LTD. |