Data / Medical devices / United States / Tri-Anim Health Services, Inc.
Tri-Anim Health Services, Inc.: FDA-registered device maker in Dublin, OH, United States, 3 510(k) clearances
Tri-Anim Health Services, Inc. is registered with the FDA (registration 3010683054) in Dublin, OH, United States. It lists 6 device types. The FDA files 3 510(k) clearances under its listings, the newest dated November 16, 2022. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3010683054
- Address
- Regulatory Affairs Department 5000 Bradenton Ave, Dublin, OH, United States, 43017
- Owner or operator
- Sarnova HC, LLC (9045180)
- Roles
- Specification developer
- First device listed
- August 29, 2023
- Registered through
- 2027
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase | CCK | 2 | Specification developer | accessdata.fda.gov |
| Device, Fixation, Tracheal Tube | CBH | 1 | Specification developer | accessdata.fda.gov |
| Laryngoscope, Rigid | CCW | 1 | Specification developer | accessdata.fda.gov |
| Protector, Skin Pressure | FMP | 1 | Specification developer | accessdata.fda.gov |
| Set, Tubing And Support, Ventilator (W Harness) | BZO | 1 | Specification developer | accessdata.fda.gov |
| Spirometer, Therapeutic (Incentive) | BWF | 2 | 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 |
|---|---|---|---|---|---|---|
| November 16, 2022 | K220533 | Endoscopy Oxygen Mask | CCK | Substantially Equivalent | Engineered Medical Systems, Inc. | accessdata.fda.gov |
| February 21, 2017 | K163091 | VibraPEP | BWF | Substantially Equivalent | Medica Holdings, LLC | accessdata.fda.gov |
| March 25, 2016 | K153441 | VibraPEP | BWF | Substantially Equivalent | Medica Holdings, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Spirometer, Therapeutic (Incentive)
- All makers of Set, Tubing And Support, Ventilator (W Harness)
- All makers of Protector, Skin Pressure
- All makers of Device, Fixation, Tracheal Tube
- All makers of Laryngoscope, Rigid
- All makers of Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
Updated November 16, 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.