Toefx, Inc.
CanadaFDA applicant, unverified
Toefx, Inc. is a medical device manufacturer, with 4 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) as of 13 Nov 2026.
- Devices
- 4
Registry facts
- Registries
- FDA GUDID 3
- FDA 510(k) 1
- Device classes
- FDA Class II 3
- FDA Class I 1
- Sites and related companies
- Toefx Inc. Canada
- Identifiers
- DUNS 202099070
What Toefx, Inc. makes
Toefx, Inc. manufactures nail laser phototherapy units designed for treating nail conditions using light-based therapy. The TFX-LT2000 Therapy Light is a key product in this category, targeting issues such as fungal infections or discoloration in nails through controlled light exposure.
The company’s devices fall under FDA Class II regulation and are listed in the FDA’s 510(k) and UDI registries.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
TFX-LT2000 Therapy Light Ref K211265
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 202099070
Sites
- Toefx Inc. CAFEI 3030926983 0 devices
Frequently asked questions
How many devices does Toefx, Inc. have in the registry?
The registry currently lists 4 devices for Toefx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Toefx, Inc.'s devices?
Among its 4 most recently registered devices, Toefx, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Toefx, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Toefx, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Toefx, Inc. in the registry?
The most recently registered devices listed for Toefx, Inc. include FungalBlue TFX-CTS, RedRevive TFX LT1000N and TFX-LT2000 Therapy Light.