Trylon Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 7
What Trylon Corp. makes
Trylon Corp. manufactures dental and pelvic examination tools, including illuminated dental specula (SPECULITE), comprehensive oral exam trays (ORALLITE), and oral exam kits (VIZILITE-BLUE). Their portfolio also includes pelvic exam trays (PAP PLUS) and cervical biopsy instruments (SPIRABRUSH CX).
The company’s devices are regulated under FDA Class I and Class II classifications, with several authorised via the 510(k) pathway. They are based in the United States and listed in the FDA’s 510(k) registry.
Catalogue
Speculite Ref K953364
510(k) 510(k)Orallite Comprehensive Exam Tray Ref K012070
510(k) 510(k)Speculite/Orallite Ref K003995
510(k) 510(k)Speculite Ref K963391
510(k) 510(k)Vizilite-Blue Oral Exam Kit Ref K033033
510(k) 510(k)- 510(k) 510(k)
Spirabrush Cx Biopsy Instrument Ref K011488
510(k) 510(k)
Frequently asked questions
How many devices does Trylon Corp. have in the registry?
The registry currently lists 7 devices for Trylon Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Trylon Corp.'s devices?
Among its 7 most recently registered devices, Trylon Corp. has devices listed in FDA 510(k) (7 devices).
What risk classes do Trylon Corp.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Trylon Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Trylon Corp. in the registry?
The most recently registered devices listed for Trylon Corp. include SPECULITE, ORALLITE COMPREHENSIVE EXAM TRAY, SPECULITE/ORALLITE and VIZILITE-BLUE ORAL EXAM KIT.