Suros Surgical Systems, Inc. A Hologic Company
United StatesFDA applicant, unverified
- Devices
- 2
What Suros Surgical Systems, Inc. A Hologic Company makes
Suros Surgical Systems, Inc. manufactures biopsy site identification and marking systems, including the SECURMARK Biopsy Site Identification System and the SECURMARK Biopsy Site Marking System. These devices are designed to aid in the precise localization and identification of biopsy sites to reduce complications and improve procedural accuracy.
The company’s portfolio is regulated under Class II medical devices in the United States, with products listed via the FDA’s 510(k) clearance process. The devices are based in the US.
Catalogue
Securmark Biopsy Site Identification System Ref K072913
Regimes: 510(k) Registry: 510(k)Securmark Biopsy Site Marking System Ref K102608
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Suros Surgical Systems, Inc. A Hologic Company have in the registry?
The registry currently lists 2 devices for Suros Surgical Systems, Inc. A Hologic Company. Devices recorded under merged duplicate company entries are counted once.
Which registries list Suros Surgical Systems, Inc. A Hologic Company's devices?
Among its 2 most recently registered devices, Suros Surgical Systems, Inc. A Hologic Company has devices listed in FDA 510(k) (2 devices).
What risk classes do Suros Surgical Systems, Inc. A Hologic Company's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Suros Surgical Systems, Inc. A Hologic Company's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Suros Surgical Systems, Inc. A Hologic Company in the registry?
The most recently registered devices listed for Suros Surgical Systems, Inc. A Hologic Company include SECURMARK BIOPSY SITE IDENTIFICATION SYSTEM and SECURMARK BIOPSY SITE MARKING SYSTEM.