Truline Instruments, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Truline Instruments, Inc. makes
Truline Instruments, Inc. manufactures eye surgery instruments designed for use in ophthalmic procedures.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Knife, Ophthalmic Ref K871285
510(k) 510(k)Eye Surgery Instrument Ref K840101
510(k) 510(k)
Frequently asked questions
How many devices does Truline Instruments, Inc. have in the registry?
The registry currently lists 2 devices for Truline Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Truline Instruments, Inc.'s devices?
Among its 2 most recently registered devices, Truline Instruments, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Truline Instruments, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Truline Instruments, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Truline Instruments, Inc. in the registry?
The most recently registered devices listed for Truline Instruments, Inc. include KNIFE, OPHTHALMIC and EYE SURGERY INSTRUMENT.