This page includes the latest FDA filings for Petertam. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Registration Number | 3003927385 | ||||||||
FEI Number | 3003927385 | ||||||||
Name | PETERTAM | ||||||||
Owner & Operator | Blue Ocean Innovation Limited | ||||||||
Contact Address | Unit 50, 8/F Wah Lok Industrial Centre P 31-35 Shan Mei Street. FOTAN HK-NA -- HK | ||||||||
Official Correspondent |
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US Agent |
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Importing Logistics Registration |
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Importing Logistics Registration |
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Registration Status | 1 | ||||||||
Initial Importer | N | ||||||||
Registration Expiration | 2020-04-25 | ||||||||
Registration Address | 5 Harcourt Newport Beach, CA 92657 US | ||||||||
Establishment Type | Manufacture Medical Device for Another Party (Contract Manufacturer) |
Device Company | Device | Date |
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PETERTAM [Blue Ocean Innovation Limited] | Innovo (JDI #525) | 2019-02-27 |
PETERTAM [Blue Ocean Innovation Limited] | BioStamp nPoint (JDI #558) | 2018-05-14 |
PETERTAM [Blue Ocean Innovation Limited] | Kintinuum (JDI #558) | 2018-05-10 |
PETERTAM [Blue Ocean Innovation Limited] | SAFIRA (JDI #549) | 2016-09-21 |
PETERTAM [Blue Ocean Innovation Limited] | Slenderton Connect Abs (JDI #551) | 2015-11-12 |