Spectro Industries, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Spectro Industries, Inc. makes
Spectro Industries, Inc. manufactures the SURGISMOKE, a device designed to reduce or monitor surgical smoke during procedures, and the Kanievski Sensory Aid or Device, intended for sensory assistance applications.
The company’s portfolio includes Class II and Unclassified (U) devices, with products listed under the FDA’s 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Surgismoke Ref K896822
Regimes: 510(k) Registry: 510(k)Kanievski Sensory Aid Or Device Ref K843433
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spectro Industries, Inc. have in the registry?
The registry currently lists 2 devices for Spectro Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spectro Industries, Inc.'s devices?
Among its 2 most recently registered devices, Spectro Industries, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Spectro Industries, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Spectro Industries, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spectro Industries, Inc. in the registry?
The most recently registered devices listed for Spectro Industries, Inc. include SURGISMOKE and KANIEVSKI SENSORY AID OR DEVICE.