Embolx Inc

FDA Filings

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

FDA Registration(s)
Registration Number3011660785
FEI Number3011660785
NameEMBOLX INC.
Owner & OperatorEmbolx Inc.
Contact Address530 Lakeside Dr Ste 200
Sunnyvale CA 94085 US
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address530 Lakeside Dr Ste 200
Sunnyvale, CA 94085 US
Establishment TypeComplaint File Establishment per 21 CFR 820.198



FDA Filings

Device
Company
DeviceDate
Embolx, Inc.
Sniper SBC0629-STR-1652022-05-26
EMBOLX, INC.
Sniper SA-00902019-04-09
EMBOLX, INC.
Sniper® SBC0629-KTP-1502019-04-09
EMBOLX, INC.
Sniper® SBC0629-KTP-1302019-04-09
EMBOLX, INC.
Sniper® SBC0629-KTP-1102019-04-09
EMBOLX, INC.
Sniper SBC0629-STR-1102019-04-09
EMBOLX, INC.
Sniper SBC0629-STR-1302019-04-09
EMBOLX, INC.
Sniper SBC0629-STR-1502019-04-09
EMBOLX, INC.
Sniper SBC0629-1502019-04-09
EMBOLX, INC.
Sniper SBC0629-1302019-04-09
EMBOLX, INC.
Sniper SBC0629-1102019-04-09
Embolx, Inc
Sniper Infusion Catheter With Balloon Occlusion2018-06-08
EMBOLX INC.
Sniper Infusion Catheter with Balloon Occlusion2015-06-29
EMBOLX, INC.
Occlusion Balloon Catheter2015-05-31

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