Dalton Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Dalton Technology, Inc. makes
Dalton Technology, Inc. manufactures flexible surgical instruments, including a flexible screwdriver designed for precise, minimally invasive procedures, and a modular drilling system for controlled tissue penetration in surgical applications.
The company’s products are classified as Class I medical devices under FDA regulations, with individual devices authorised through the 510(k) clearance pathway. Dalton Technology, Inc. is based in the United States.
Catalogue
Dalton Technology Flexible Screwdriver Ref K901166
Regimes: 510(k) Registry: 510(k)Modular Flexible Drilling System Ref K901165
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dalton Technology, Inc. have in the registry?
The registry currently lists 2 devices for Dalton Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dalton Technology, Inc.'s devices?
Among its 2 most recently registered devices, Dalton Technology, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Dalton Technology, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Dalton Technology, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dalton Technology, Inc. in the registry?
The most recently registered devices listed for Dalton Technology, Inc. include DALTON TECHNOLOGY FLEXIBLE SCREWDRIVER and MODULAR FLEXIBLE DRILLING SYSTEM.