Data / Medical devices / United States / Peerbridge Health, Inc.
Peerbridge Health, Inc.: FDA-registered device maker in Franklin, TN, United States, 1 510(k) clearance
Peerbridge Health, Inc. is registered with the FDA (registration 3014111150) in Franklin, TN, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 27, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014111150
- Address
- 1000 Corporate Centre Dr Ste 390, Franklin, TN, United States, 37067
- Owner or operator
- Peerbridge Health, Inc. (10055165)
- Roles
- Manufacturer, Specification developer
- First device listed
- October 26, 2017
- Registered through
- 2026
- Brand names listed
- Peerbridge Adhesive Electrode, Peerbridge Cor, Peerbridge Cor(TM) System, Peerbridge Portal, Peerbridge ReportGen, Peerbridge Workstation
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrode, Electrocardiograph | DRX | 2 | Specification developer | accessdata.fda.gov |
| Medical Device Data System | OUG | 1 | Manufacturer | accessdata.fda.gov |
| Recorder, Magnetic Tape, Medical | DSH | 2 | Manufacturer, Specification developer | 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 |
|---|---|---|---|---|---|---|
| September 27, 2017 | K171936 | Peerbridge Cor(TM) System | DSH | Substantially Equivalent | Peerbridge Health, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Medical Device Data System
- All makers of Recorder, Magnetic Tape, Medical
- All makers of Electrode, Electrocardiograph
Updated September 27, 2017. 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.