Implicity, Inc.
United StatesFDA applicant, unverified
Part of Implicity
Implicity, Inc. is a medical device manufacturer, with 4 devices listed in FDA 510(k) and FDA GUDID (FDA Class II) as of 13 Nov 2026.
- Devices
- 4
Registry facts
- Registries
- FDA 510(k) 3
- FDA GUDID 1
- Device classes
- FDA Class II 4
- Sites and related companies
- Identifiers
- DUNS 118346169
Catalogue
ILR ECG Analyzer (IM007) Ref K253463
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: GUDID
IM007 Ref K210543
Regimes: 510(k) Registry: 510(k)SignalHF (IM008) Ref K230842
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 118346169
Frequently asked questions
How many devices does Implicity, Inc. have in the registry?
The registry currently lists 4 devices for Implicity, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Implicity, Inc.'s devices?
Among its 4 most recently registered devices, Implicity, Inc. has devices listed in FDA 510(k) (3 devices) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Implicity, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Implicity, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Implicity, Inc. in the registry?
The most recently registered devices listed for Implicity, Inc. include ILR ECG Analyzer (IM007), SignalHF V1.0.2, IM007 and SignalHF (IM008).