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Sign in to claim this brandFacet Technologies, LLC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 3900 North Commerce Drive, Atlanta, GA, 30344
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3011617315
- DUNS Number
- —
Catalogue (32)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Carefine | 1100039 | FDA UDI | Class II | Active |
| Carefine | 1100015 | FDA UDI | Class II | Active |
| Facet Medical Technologies | 0110001 | FDA UDI | Class II | Active |
| Carefine | 1100000 | FDA UDI | Class II | Active |
| Carefine | 1100029 | FDA UDI | Class II | Active |
| Carefine | 1100013 | FDA UDI | Class II | Active |
| Carefine | 1100017 | FDA UDI | Class II | Active |
| Facet Medical Technologies | 0108002 | FDA UDI | Class I | Active |
| Quintapoint | 10167250 | FDA UDI | Class II | Active |
| Carefine | 1100007 | FDA UDI | Class II | Active |
| Carefine | 1100031 | FDA UDI | Class II | Active |
| Facet Medical Technologies | 0108001 | FDA UDI | Class I | Active |
| Carefine | 1100003 | FDA UDI | Class II | Active |
| Quintapoint | 10167252 | FDA UDI | Class II | Active |
| Quintapoint | 10167251 | FDA UDI | Class II | Active |
| Carefine | 1100037 | FDA UDI | Class II | Active |
| Carefine | 1100041 | FDA UDI | Class II | Active |
| Facet Medcial Technologies | 0110002 | FDA UDI | Class II | Active |
| Carefine | 1100027 | FDA UDI | Class II | Active |
| Quintapoint | 10167253 | FDA UDI | Class II | Active |
| SureSeal | Large | FDA UDI | Class I | Active |
| SureSeal | Extra Large | FDA UDI | Class I | Active |
| Carefine | 1100033 | FDA UDI | Class II | Active |
| Carefine | 1100035 | FDA UDI | Class II | Active |
| Carefine Pen Needle | K133100 | FDA 510(k) | Class II | Active |
| NeatNick Heel Safety Lancet | K223370 | FDA 510(k) | Class II | Active |
| Facet 28G Universal Lancet | K221433 | FDA 510(k) | Class II | Active |
| Facet Aurora Reusable Lancet Base | K232912 | FDA 510(k) | Class II | Active |
| Carefine Pen Needle With Quintapoint And Superpoint | K140568 | FDA 510(k) | Class II | Active |
| Facet Blood Lancets | K222539 | FDA 510(k) | Class II | Active |
| Facet Manatee Reusable Lancing Base | K223099 | FDA 510(k) | Class II | Active |
| Carefine Pen Needle Family Including Quintapoint And Superpoint | K141749 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Jul 18, 2008 | Z-0174-2009 | — | terminated | The Alternate Site Cap was not included in the package as indicated on the labeling. |