Data / Medical devices / United States / Best Nomos
Best Nomos: FDA-registered device maker in Pittsburgh, PA, United States, 5 510(k) clearances
Best Nomos is registered with the FDA (registration 2434141) in Pittsburgh, PA, United States. It lists 4 device types. The FDA files 5 510(k) clearances under its listings, the newest dated May 6, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2434141
- Address
- 1 Best Drive, Pittsburgh, PA, United States, 15202
- Owner or operator
- Best NOMOS (2434141)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- January 8, 2009
- Registered through
- 2026
- Brand names listed
- CORVUS 15, Precision Stepper, Sonalis Ultrasound System, Treatment Planning System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Applicator, Radionuclide, Manual | IWJ | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| System, Imaging, Pulsed Echo, Ultrasonic | IYO | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| System, Planning, Radiation Therapy Treatment | MUJ | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Transducer, Ultrasonic, Diagnostic | ITX | 2 | Complaint file establishment, Manufacturer | 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 |
|---|---|---|---|---|---|---|
| May 6, 2021 | K211034 | Corvus Radiation Therapy Planning System | MUJ | Substantially Equivalent | Best Nomos | accessdata.fda.gov |
| February 19, 2010 | K100204 | SONALIS | ITX | Substantially Equivalent | Smith Associates | accessdata.fda.gov |
| February 9, 2005 | K043189 | SONALIS, MODEL 2000 | IYO | Substantially Equivalent | 3g Ultrasound, Inc. | accessdata.fda.gov |
| December 11, 1998 | K981678 | STRATA, MODEL V.O.95 | MUJ | Substantially Equivalent | Rosses Medical Systems | accessdata.fda.gov |
| January 2, 1998 | K973786 | NORTHWEST RADIATION THERAPY PRODUCTS, PRECISION STEPPER AND GUIDE | IWJ | Substantially Equivalent | Nw Radiation Therapy Products | accessdata.fda.gov |
Compare with other makers
- All makers of Transducer, Ultrasonic, Diagnostic
- All makers of System, Imaging, Pulsed Echo, Ultrasonic
- All makers of System, Planning, Radiation Therapy Treatment
- All makers of System, Applicator, Radionuclide, Manual
Updated May 6, 2021. 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.