Doran Instruments, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Doran Instruments, Inc. makes
Doran Instruments, Inc. manufactures the Maculoscope™, a handheld retinal imaging device for ophthalmologic examinations, and the GoldLens™, a specialized lens for slit-lamp biomicroscopy used in eye care diagnostics.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) clearance pathway. These devices are listed in the FDA’s 510(k) registry. Doran Instruments, Inc. is headquartered in the United States.
Catalogue
Maculoscope(Tm) Ref K863956
510(k) 510(k)Goldlens(Tm) Ref K913239
510(k) 510(k)
Frequently asked questions
How many devices does Doran Instruments, Inc. have in the registry?
The registry currently lists 2 devices for Doran Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Doran Instruments, Inc.'s devices?
Among its 2 most recently registered devices, Doran Instruments, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Doran Instruments, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Doran Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Doran Instruments, Inc. in the registry?
The most recently registered devices listed for Doran Instruments, Inc. include MACULOSCOPE(TM) and GOLDLENS(TM).