Data / Medical devices / United States / Current Health Inc
Current Health Inc: FDA-registered device maker in Rochester, NY, United States, 1 510(k) clearance
Current Health Inc is registered with the FDA (registration 3044754336) in Rochester, NY, United States. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 1, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3044754336
- Address
- 2400 Mount Read Blvd Dock 55 Building 205, Rochester, NY, United States, 14615
- Owner or operator
- Current Health Ltd (10059040)
- Roles
- Repackager or relabeler
- First device listed
- November 14, 2022
- Registered through
- 2026
- Brand names listed
- Current Health Wearable Monitoring System G2
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Continuous Measurement Thermometer | FLL | 2 | Repackager or relabeler | accessdata.fda.gov |
| Monitor, Breathing Frequency | BZQ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Oximeter | DQA | 2 | Repackager or relabeler | accessdata.fda.gov |
| Spirometer, Diagnostic | BZG | 2 | Repackager or relabeler | accessdata.fda.gov |
| System, Network And Communication, Physiological Monitors | MSX | 2 | Repackager or relabeler | accessdata.fda.gov |
| Transmitters And Receivers, Physiological Signal, Radiofrequency | DRG | 2 | Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 1, 2022 | K222550 | Current Health System | MSX | Substantially Equivalent | Current Health , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Transmitters And Receivers, Physiological Signal, Radiofrequency
- All makers of Spirometer, Diagnostic
- All makers of System, Network And Communication, Physiological Monitors
- All makers of Monitor, Breathing Frequency
- All makers of Continuous Measurement Thermometer
- All makers of Oximeter
Updated November 1, 2022. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.