Mtd, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Mtd, Inc. makes
Mtd, Inc. makes patient restraint systems, armboards, cassette holders for imaging systems, arthrostress devices, and medical image management devices for vision tools.
The company's devices are classified as Class I and Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Patient Restraint System Ref K771659
Regimes: 510(k) Registry: 510(k)Armboard Ref K833559
Regimes: 510(k) Registry: 510(k)The Mtd Vara Set Casette Holder Ref K791374
Regimes: 510(k) Registry: 510(k)Arthrostress Ref K772321
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mtd, Inc. have in the registry?
The registry currently lists 5 devices for Mtd, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mtd, Inc.'s devices?
Among its 5 most recently registered devices, Mtd, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Mtd, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Mtd, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mtd, Inc. in the registry?
The most recently registered devices listed for Mtd, Inc. include PATIENT RESTRAINT SYSTEM, ARMBOARD, THE MTD VARA SET CASETTE HOLDER and ARTHROSTRESS.