CODIAGNOSTICS
Registration 3014214006FEI 3014214006Salt Lake City, UT
Owner/operator: Co-Diagnostics, Inc.
- Complaint File Establishment per 21 CFR 820.198
- Manufacture Device in the United States for Export Only
- Repack or Relabel Medical Device
Renewal due by December 31, 2026
Registered through 2026. Renew between October 1 and December 31, 2026, to stay registered for 2027.
90days left in the window
The 2026 window
- Oct 1Window opens91 days left
- Nov 3Where you stand58 days left
- Dec 1Our pay-by date30 days left
- Dec 15Two weeks left16 days left
- Dec 23Holiday week8 days left
- Dec 29Two days left2 days left
- Dec 31Window closes0 days left
- FDA fee, FY2027
- $13,785
- Our pay-by suggestion
- Dec 1
- Listed devices
- 8
- Added, last 12 months
- 0
FDA sets who pays the fee and who may qualify for a waiver; its fee page says so. The fee is paid only on FDA’s own fee site. Never through us. FDA’s fee page
The steps, in order
Pay FDA's annual feeYou
Order and pay the FY2027 establishment fee on FDA's Device Facility User Fee site. FDA emails you a PIN when you order.
FDA: registration and listing payment processWait for the payment confirmation numberYou
FDA emails a Payment Confirmation Number (PCN) once the payment processes, which FDA says typically takes several days. That is why we suggest paying by December 1.
FDA: registration and listing payment processRenew the registration in FDA's systemYou
Sign in to FDA's Unified Registration and Listing System (FURLS), complete the annual registration and apply your PIN and PCN. FDA does not count the registration as complete until both are applied.
FDA: device registration and listingReview every listingYou
In the same window, review each listing on file and report any changes, deletions and new listings. Your Listing Review Sheet puts every listing on one page.
FDA: device registration and listing
Every listed device 8
| Code | Device | Class | Regulation | Premarket |
|---|---|---|---|---|
| NSU | CoDx Box CyclerInstrumentation For Clinical Multiplex Test Systems | Class 2 | 21 CFR 862.2570 | — |
| MWA | Logix Smart MTBSystem, Nucleic Acid Amplification, Mycobacterium Tuberculosis Complex | Class 2 | 21 CFR 866.3372 | — |
| PEU | Mycobacterium Tuberculosis Drug Resistance Panel KitSystem, Nucleic Acid-Based, Mycobacterium Tuberculosis Complex, Resistance Marker, Direct Specimen | Class 2 | 21 CFR 866.3373 | — |
| QLT | Logix Smart ABC (Influenza A/B, SARS-CoV-2)Covid-19 Multi-Analyte Respiratory Panel Nucleic Acid Devices | Not classified | — | — |
| PCY | Logix Smart DENVInvestigational Use Only - Microbiology | Not classified | — | — |
| QJR | Logix Smart Coronavirus Disease 2019 (COVID-19) - 100 reactionsReagents, 2019-Novel Coronavirus Nucleic Acid | Not classified | — | — |
| POA | Logix Smart ZDC (ZIKV, DENV, CHIKV)Reagents, Zika Virus Nucleic Acid | Not classified | — | — |
| OTT | Logix Smart DENVResearch Use Only/Microbiology | Not classified | — | — |
What changed
Nothing added in the last twelve months, and no change seen on the record yet.