Davol, Inc., A Subsidiary of C.R. Bard, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Davol, Inc., A Subsidiary of C.R. Bard, Inc. makes
Davol, Inc. manufactures the Phasix ST Umbilical Hernia Patch, a surgical mesh product designed for the repair of umbilical hernias. The device is intended for use in open surgical procedures to reinforce abdominal wall defects.
The Phasix ST Umbilical Hernia Patch is classified as a Class II medical device in the U.S. and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Phasix ST Parastomal Hernia Mesh Ref K261543
Regimes: 510(k) Registry: 510(k)3DMax Light Mesh Ref K241250
Regimes: 510(k) Registry: 510(k)Onflex™ Mesh Ref K251955
Regimes: 510(k) Registry: 510(k)Bard 3DMax Mesh Ref K233402
Regimes: 510(k) Registry: 510(k)Phasix ST Umbilical Hernia Patch Ref K243241
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Davol, Inc., A Subsidiary of C.R. Bard, Inc. have in the registry?
The registry currently lists 5 devices for Davol, Inc., A Subsidiary of C.R. Bard, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Davol, Inc., A Subsidiary of C.R. Bard, Inc.'s devices?
Among its 5 most recently registered devices, Davol, Inc., A Subsidiary of C.R. Bard, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Davol, Inc., A Subsidiary of C.R. Bard, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Davol, Inc., A Subsidiary of C.R. Bard, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Davol, Inc., A Subsidiary of C.R. Bard, Inc. in the registry?
The most recently registered devices listed for Davol, Inc., A Subsidiary of C.R. Bard, Inc. include Phasix ST Parastomal Hernia Mesh, 3DMax Light Mesh, Onflex™ Mesh and Bard 3DMax Mesh.