Data / Medical devices / United States / Nexus CMF
Nexus CMF: FDA-registered device maker in Salt Lake City, UT, United States, 1 510(k) clearance
Nexus CMF is registered with the FDA (registration 3009702671) in Salt Lake City, UT, United States. It lists 15 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 18, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009702671
- Address
- 2825 E. Cottonwood Parkway Suite 330, Salt Lake City, UT, United States, 84121
- Owner or operator
- Nexus CMF (10039882)
- Roles
- Complaint file establishment, Repackager or relabeler, Specification developer
- First device listed
- February 17, 2012
- Registered through
- 2026
- Brand names listed
- Bone File, Nexus Trocar, Rongeur Forceps, Scissors, TMJ Drape/Fluid Collection Kit, Tray, surgical, Tubing
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Arthroscopic | NBH | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Arthroscope | HRX | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Camera, Surgical And Accessories | KQM | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Drape, Surgical, Exempt | PUI | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| File | HTP | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Forceps | HTD | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Knife, Orthopedic | HTS | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Needle, Aspiration And Injection, Disposable | GAA | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Probe | HXB | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Rongeur | HTX | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Scissors, Orthopedic, Surgical | HRR | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Template | HWT | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Tray, Surgical | LRP | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Trocar, Ent | KTE | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Tubing, Pressure And Accessories | BYX | 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 |
|---|---|---|---|---|---|---|
| March 18, 2008 | K080560 | HENKE SASS WOLF OF AMERICA ARTHROSCOPE | HRX | Substantially Equivalent | Henke Sass Wolf of America, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Scissors, Orthopedic, Surgical
- All makers of Probe
- All makers of Trocar, Ent
- All makers of Arthroscope
- All makers of Camera, Surgical And Accessories
- All makers of Knife, Orthopedic
Updated March 18, 2008. 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.