Full Spectrum, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
What Full Spectrum, Inc. makes
Full Spectrum, Inc. manufactures laparoscopic probes designed for use with specific fiber optic models, including ULE and ULE-overclad fibers. The company produces probes with varying fiber diameters (100, 200, and 400) and a ULE-overclad fiber model (201). These devices are intended for minimally invasive surgical applications.
The company’s products fall under FDA Class II devices and are listed via 510(k) clearance. The portfolio is regulated under US medical device laws, and the manufacturer is based in the United States.
Catalogue
- 510(k) 510(k)
Full Spectrum Ule-Overclad Fiber: Model 201 Ref K955862
510(k) 510(k)- 510(k) 510(k)
Frequently asked questions
How many devices does Full Spectrum, Inc. have in the registry?
The registry currently lists 3 devices for Full Spectrum, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Full Spectrum, Inc.'s devices?
Among its 3 most recently registered devices, Full Spectrum, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Full Spectrum, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Full Spectrum, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Full Spectrum, Inc. in the registry?
The most recently registered devices listed for Full Spectrum, Inc. include (FSI) LAPAROSCOPIC PROBE FOR ALL FSI ULE FF101 FIBERS. MODEL FSI FF101-LP-XXX, WHERE XXX = FIBER DIAMETERS 100, 200, 400, FULL SPECTRUM ULE-OVERCLAD FIBER: MODEL 201 and FSI LAPAROSCOPIC PROBE FOR ALL FSI ULE-OVERCLAD FF201 FIBERS.