Data / Medical devices / United States / Physician Recommended Nutriceuticals PRN
Physician Recommended Nutriceuticals PRN: FDA-registered device maker in Blue Bell, PA, United States, 2 510(k) clearances
Physician Recommended Nutriceuticals PRN is registered with the FDA (registration 3006984486) in Blue Bell, PA, United States. It lists 5 device types. The FDA files 2 510(k) clearances under its listings, the newest dated July 24, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006984486
- Address
- 960 Harvest Drive Ste B205, Blue Bell, PA, United States, 19422
- Owner or operator
- Physician Recommended Nutriceuticals PRN (10083471)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- January 17, 2025
- Registered through
- 2026
- Brand names listed
- Avenova, Eye Love, Eyeeco, PRN, ZX Pro
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Adaptometer (Biophotometer), Software-Based Data Acquisition And Stimulus Generation | OUM | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Dressing, Wound, Drug | FRO | U | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Pack, Heat, Moist | IMA | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Pack, Hot Or Cold, Reusable | IME | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) | HOY | 1 | Complaint file establishment, 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 |
|---|---|---|---|---|---|---|
| July 24, 2013 | K131542 | NEUTROPHASE(R) SKIN AND WOUND CLEANSER OTC | FRO | Substantially Equivalent | Novabay Pharmaceuticals, Inc. | accessdata.fda.gov |
| September 28, 2007 | K071056 | NEUTROPHASE WOUND CLEANSER | FRO | Substantially Equivalent | Novabay Pharmaceuticals | accessdata.fda.gov |
Compare with other makers
- All makers of Dressing, Wound, Drug
- All makers of Adaptometer (Biophotometer), Software-Based Data Acquisition And Stimulus Generation
- All makers of Pack, Heat, Moist
- All makers of Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)
- All makers of Pack, Hot Or Cold, Reusable
Updated July 24, 2013. 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.