ORASURE TECHNOLOGIES INC.
Registration 3004142665FEI 3004142665BETHLEHEM, PA
Owner/operator: ORASURE TECHNOLOGIES, INC.
- Manufacture Medical Device
- Manufacture Medical Device for Another Party (Contract Manufacturer)
Renewal due by December 31, 2026
Registered through 2026. Renew between October 1 and December 31, 2026, to stay registered for 2027.
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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
- 10
- Added, last 12 months
- 1
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 10
| Code | Device | Class | Regulation | Premarket |
|---|---|---|---|---|
| QSS | OraQuick HIV Self-TestHiv Self-Tests | Class 3 | — | BP120001 |
| MZO | OraQuick HCV Rapid Antibody TestAssay, Enzyme Linked Immunosorbent, Hepatitis C Virus | Class 2 | 21 CFR 866.3169 | P080027 |
| SIH | Colli-Pee Dx Urine Collection KitDevice For Home Collection And Transport Of Specimens By Lay Users For Use In A Cleared Non-Viral Sti Molecular AssayAdded Jul 20, 2026 | Class 2 | 21 CFR 866.2920 | — |
| QID | OraQuick Ebola Rapid Antigen TestDevice To Detect Antigens Of Biothreat Microbial Agents In Human Clinical Specimens | Class 2 | 21 CFR 866.4002 | DEN190025 |
| QPO | OMNIgene-GUT (OMD-200)Device To Preserve And Stabilize Relative Abundances Of Microbial Nucleic Acids In Clinical Samples | Class 2 | 21 CFR 866.2952 | — |
| OYJ | ORAcollect DNA (OCR-100)Dna Specimen Collection, Saliva | Class 2 | 21 CFR 862.1675 | — |
| OYJ | ORAcollect Dx (OCD-100, OCD-100A)Dna Specimen Collection, Saliva | Class 2 | 21 CFR 862.1675 | — |
| QSU | OraQuick ADVANCE Rapid HIV 1/2Point Of Care Hiv Serology Diagnostic And/Or Supplemental Test | Class 2 | 21 CFR 866.3956 | BP010047 |
| QSU | OraSure HIV-1 Oral Specimen Collection DevicePoint Of Care Hiv Serology Diagnostic And/Or Supplemental Test | Class 2 | 21 CFR 866.3956 | BP910001 |
| QKP | InteliSwab COVID-19 Rapid TestCoronavirus Antigen Detection Test System. | Not classified | — | — |
What changed
- Jul 20, 2026Listing added: SIH — Colli-Pee Dx Urine Collection Kit