Triton Technology, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
What Triton Technology, Inc. makes
Triton Technology, Inc. manufactures diagnostic and procedural medical devices, including the TRITON Model 100 Pulsed Doppler Blood Flowmeter for vascular assessments, a Tissue/Polyp Trap System for endoscopic procedures, a Multiple Biopsy Device (MBX) for tissue sampling, and a Suction Guillotine Device for controlled tissue excision.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
Triton Model 100 Pulsed Doppler Blood Flowmeter Ref K881303
510(k) 510(k)Tissue/Polyp Trap System Ref K902883
510(k) 510(k)Multiple Biopsy Device-Mbx Ref K911448
510(k) 510(k)Suction Guillotine Device Ref K932142
510(k) 510(k)
Frequently asked questions
How many devices does Triton Technology, Inc. have in the registry?
The registry currently lists 4 devices for Triton Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Triton Technology, Inc.'s devices?
Among its 4 most recently registered devices, Triton Technology, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Triton Technology, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Triton Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Triton Technology, Inc. in the registry?
The most recently registered devices listed for Triton Technology, Inc. include TRITON MODEL 100 PULSED DOPPLER BLOOD FLOWMETER, TISSUE/POLYP TRAP SYSTEM, MULTIPLE BIOPSY DEVICE-MBX and SUCTION GUILLOTINE DEVICE.