Data / Medical devices / United States / Koning Corporation
Koning Corporation: FDA-registered device maker in Norcross, GA, United States, 1 PMA approval
Koning Corporation is registered with the FDA (registration 3008513054) in Norcross, GA, United States. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated January 14, 2015. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008513054
- Address
- 5555 Oakbrook Pkwy Ste 640, Norcross, GA, United States, 30093
- Owner or operator
- Koning Corporation (10033113)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- January 22, 2016
- Registered through
- 2026
- Brand names listed
- Koning Corporation, Norcross, Georgia
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cross-Sectional Mammographic Xray System | OLQ | 3 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| January 14, 2015 | P130025 | KONING BREAST CT (MODEL CBCT1000) | OLQ | 3 | October 12, 2023 | accessdata.fda.gov |
Updated October 12, 2023. 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.