Myriad Lase, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Myriad Lase, Inc. makes
Myriad Lase, Inc. manufactures reusable and disposable optical fibers designed for laser-based medical procedures. Their products include straight-tipped and sidefire-tipped fibers, such as the TBN-tipped, Sidefire-tipped, and Straightfire variants, which are used in applications requiring precise laser delivery.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company’s portfolio is listed in the FDA’s 510(k) database, reflecting their regulatory standing in the United States.
Catalogue
Tbn-Tipped Optical Fiber Ref K952113
Regimes: 510(k) Registry: 510(k)Sidefire - Tipped Reusable Optical Fibers Ref K952733
Regimes: 510(k) Registry: 510(k)Myriadlase Sidefire-Tipped Optical Fiber Ref K920553
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Myriad Lase, Inc. have in the registry?
The registry currently lists 4 devices for Myriad Lase, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Myriad Lase, Inc.'s devices?
Among its 4 most recently registered devices, Myriad Lase, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Myriad Lase, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Myriad Lase, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Myriad Lase, Inc. in the registry?
The most recently registered devices listed for Myriad Lase, Inc. include TBN-TIPPED OPTICAL FIBER, SIDEFIRE - TIPPED REUSABLE OPTICAL FIBERS, MYRIADLASE SIDEFIRE-TIPPED OPTICAL FIBER and STRAIGHTFIRE REUSABLE OPTICAL FIBERS (400, 600, 800, 1000).