Vnus Medical Technologies, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 9
- FDA recalls
- 3
At a glance
Market reach
- United States
- FDA recalls
Catalogue
Vnus Vessel And Tissue Coagulation System Ref K033547
510(k) 510(k)- 510(k) 510(k)
Modification To Vnus Closure System Ref K003092
510(k) 510(k)Vnus Closure System Ref K982816
510(k) 510(k)- 510(k) 510(k)
Vnus Closure System Ref K974521
510(k) 510(k)Vnus Rfs, Model Rfs-6-Xx (Xx = 10, 12, 13, & 15); Vnus Rfs Flex, Model Rfx-6-Xx (Xx = 10, 20, 30 & 40) Ref K052003
510(k) 510(k)Vnus Radiofrequency Generator, Model RFG2 Ref K040638
510(k) 510(k)Modification To Vnus Closure System Ref K030557
510(k) 510(k)
FDA recalls
2007
- 8 Aug 2007 Z-0542-2008 Unclassified (pre-2012) Terminated Instructions for Use change: Instructions for Use have been changed to include a modified placement recommendation.
- 8 Aug 2007 Z-0543-2008 Unclassified (pre-2012) Terminated Instructions for Use change: Instructions for Use have been changed to include a modified placement recommendation.
- 6 Mar 2007 Z-0132-2008 Unclassified (pre-2012) Terminated Sterility (package integrity) Compromised: Product sterility may be compromised due to a pinhole under the pouch foldover.
Full distribution text
Frequently asked questions
How many devices does Vnus Medical Technologies, Inc. have in the registry?
The registry currently lists 9 devices for Vnus Medical Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vnus Medical Technologies, Inc.'s devices?
Among its 9 most recently registered devices, Vnus Medical Technologies, Inc. has devices listed in FDA 510(k) (9 devices).
What risk classes do Vnus Medical Technologies, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Vnus Medical Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Vnus Medical Technologies, Inc.?
FDA recall records list 3 recalls initiated by Vnus Medical Technologies, Inc., the most recent initiated on 2007-08-08. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Vnus Medical Technologies, Inc. in the registry?
The most recently registered devices listed for Vnus Medical Technologies, Inc. include VNUS VESSEL AND TISSUE COAGULATION SYSTEM, VNUS CLOSUREFAST CATHETER, MODELS CF7-7-60 AND CF7-7-100, MODIFICATION TO VNUS CLOSURE SYSTEM and VNUS CLOSURE SYSTEM.