Technology Delivery Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Technology Delivery Systems, Inc. makes
Technology Delivery Systems, Inc. makes medical devices including semi-flex scopes and a fiber optic energy delivery system. Their products, such as the MAXIFLEX, are used for various medical procedures.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
Maxiflex - Semi Flex Scope, 25 To 65 Cm Ref K111480
Regimes: 510(k) Registry: 510(k)Maxiflex-Semi Flex Scope Ref K062725
Regimes: 510(k) Registry: 510(k)Maxiflex Fiber Optic Energy Delivery System Ref K013300
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Technology Delivery Systems, Inc. have in the registry?
The registry currently lists 3 devices for Technology Delivery Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Technology Delivery Systems, Inc.'s devices?
Among its 3 most recently registered devices, Technology Delivery Systems, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Technology Delivery Systems, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Technology Delivery Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Technology Delivery Systems, Inc. in the registry?
The most recently registered devices listed for Technology Delivery Systems, Inc. include MAXIFLEX - SEMI FLEX SCOPE, 25 TO 65 CM, MAXIFLEX-SEMI FLEX SCOPE and MAXIFLEX FIBER OPTIC ENERGY DELIVERY SYSTEM.