Biowy Corp

FDA Filings

This page includes the latest FDA filings for Biowy Corp. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3013233645
• FEI Number: 3013233645
• Name: BIOWY CORPORATION
• Owner & Operator: Biowy Corporation
• Contact Address: 27031 Vista Terrace 27002 Vista Terrace; Lake Forest CA 92630 US
• Official Correspondent:
  • Arthur - Lu
  • 1-949-3058211-x
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 27031 Vista Terrace ; Lake Forest, CA 92630 US
• Establishment Type:
  • Develop Specifications But Do Not Manufacture At This Facility
  • Manufacture Medical Device

FDA Filings

Device Company	Device	Date
GUDID 00851739007255 Biowy Corporation	Biowy Freezing Bag	2021-06-01
GUDID 00851739007248 Biowy Corporation	Biowy Freezing Bag	2021-06-01
GUDID 00851739007163 Biowy Corporation	Biowy PICC Catheter S Kit	2021-06-01
GUDID 00851739007156 Biowy Corporation	Biowy PICC Catheter S Kit	2021-06-01
GUDID 00851739007019 Biowy Corporation	Biowy Freezing Bag	2021-06-01
GUDID 00851739007002 Biowy Corporation	Biowy Freezing Bag	2021-06-01
PMN K192246 Biowy Corporation	Biowy PICC Catheter S Kit	2020-04-30
PMN BK170150 | LPZ BIOWY CORPORATION	BIOWY FREEZING BAG	2018-06-21
PMN K173956 | LJS BIOWY CORPORATION	Biowy Corporation	2018-05-25
PMN K173956 Biowy Corporation	Biowy PlCC Catheter	2018-05-21
PMN BK170150 Biowy Corporation	510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration   Follow FDA En Español Search FDA   Home Food Drugs Medical Devices	2018-05-11

Related Finance Registrations

CAGE Code	8APP3	BIOWY CORPORATION BIOWY INC.
S.A.M. Registration	8APP3 [33858426]	BIOWY CORPORATION