Viveve Inc

FDA Filings

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

FDA Registration(s)
Registration Number3013565579
FEI Number3013565579
NameViveve, Inc.
Owner & OperatorViveve, Inc.
Contact Address345 Inverness Drive South Building B, Suite 250
Englewood CO 80112 US
Official Correspondent
  • Suzon Lommel
  • x-408-6454979-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address345 Inverness Drive South Building B, Suite 250
Englewood, CO 80112 US
Establishment TypeComplaint File Establishment per 21 CFR 820.198



FDA Filings

Device
Company
DeviceDate
Viveve, Inc.
Viveve 2.0 System2022-02-02
Viveve, Inc.
Viveve 2.0 System2019-06-17
VIVEVE, INC.
COUPLING FLUID VIVCF022018-07-06
VIVEVE, INC.
CRYOGEN CANISTER VIVCC032018-07-06
VIVEVE, INC.
8 cm Treatment Tip VIVTT072018-07-06
VIVEVE, INC.
5 cm Treatment Tip S VIVTT062018-07-06
VIVEVE, INC.
5 cm Treatment Tip VIVTT052018-07-06
VIVEVE, INC.
VIVEVE Return Cable VIVRC012018-07-06
VIVEVE, INC.
VIVEVE Power Cord VIVPC0X2018-07-06
VIVEVE, INC.
VIVEVE Footswitch VIVFS012018-07-06
VIVEVE, INC.
Universal Electrosurgical Pad (3M REF 9160) VIVRP022018-07-06
VIVEVE, INC.
VIVEVE Console S VIVGE01S2018-07-06
VIVEVE, INC.
VIVEVE Console VIVGE012018-07-06
VIVEVE, INC.
VIVEVE Hand Piece S VIVHP01S2018-07-06
VIVEVE, INC.
VIVEVE Hand Piece VIVHP012018-07-06
Viveve, Inc.
Viveve System2018-04-12
Viveve Inc.
Viveve RF System, Secure2018-04-06
Viveve, Inc.
Viveve System2017-06-02
Viveve Inc.
Viveve System2016-10-06
Viveve, Inc.
Viveve System2009-12-07

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