The Witmoore Group, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What The Witmoore Group, Inc. makes
The Witmoore Group, Inc. manufactures automated biopsy tools, including the Ingress Technologies Auto BX Biopsy Needle Gun and the Ingress Technologies Auto BX Biopsy Needle. These devices are designed for core needle biopsy procedures, enabling precise tissue sampling in medical diagnostics.
The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearances. The portfolio is listed in the FDA’s 510(k) database, reflecting compliance with U.S. regulatory requirements. The manufacturer is based in the United States.
Catalogue
Ingress Technologies Auto Bx Biopsy Needle Gun Ref K896933
Regimes: 510(k) Registry: 510(k)Ingress Technologies Auto Bx Biopsy Needle Ref K896932
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Witmoore Group, Inc. have in the registry?
The registry currently lists 2 devices for The Witmoore Group, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Witmoore Group, Inc.'s devices?
Among its 2 most recently registered devices, The Witmoore Group, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do The Witmoore Group, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for The Witmoore Group, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Witmoore Group, Inc. in the registry?
The most recently registered devices listed for The Witmoore Group, Inc. include INGRESS TECHNOLOGIES AUTO BX BIOPSY NEEDLE GUN and INGRESS TECHNOLOGIES AUTO BX BIOPSY NEEDLE.