This page includes the latest FDA filings for Hakki Medical Technologies Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Hakki Medical Technologies Inc holds import registrations or U.S. agent authorizations in conjunction with the following organizations:
Registration Number | 3009034399 |
FEI Number | 3009034399 |
Name | HAKKI MEDICAL TECHNOLOGIES, INC. |
Owner & Operator | Hakki Medical Technologies, Inc. |
Contact Address | 10333 Seminole Boulevard Suite #8 Largo FL 33778 US |
Official Correspondent |
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Registration Status | 1 |
Initial Importer | Y |
Registration Expiration | 2020-04-25 |
Registration Address | 10333 Seminole Boulevard Suite #8 Largo, FL 33778 US |
Establishment Type | Develop Specifications But Do Not Manufacture At This Facility |
Device Company | Device | Date |
---|---|---|
Hakki Medical Technologies, Inc. | LotusCatheter (Lotus No Balloon Catheter) | 2020-05-21 |
HAKKI MEDICAL TECHNOLOGIES, INC. | Lotus Urinary Catheter | 2017-04-04 |
HAKKI MEDICAL TECHNOLOGIES, INC. | Hakki Urinary Catheter | 2017-04-04 |
HAKKI MEDICAL TECHNOLOGIES, INC. | HAKKI URINARY CATHETER; SIZE 14, 16, 18, 20, 22, 24, 26 FRENCH | 2011-02-07 |
NCAGE Code | 7QZ40 | HAKKI MEDICAL TECHNOLOGIES, INC. |
CAGE Code | 7QZ40 | HAKKI MEDICAL TECHNOLOGIES, INC. |
S.A.M. Registration | 7QZ40 [11406666] | HAKKI MEDICAL TECHNOLOGIES, INC. |
DUNS | 011406666 | Hakki Medical Technologies, Inc. |