PROVIDENCE MEDICAL TECHNOLOGY, INC.
Registration 3009394448FEI 3009394448Pleasanton, CA
Owner/operator: Providence Medical Technology, Inc.
- Complaint File Establishment per 21 CFR 820.198
- Develop Specifications But Do Not Manufacture At This Facility
- Manufacture Medical Device
- 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.
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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
- 12
- Added, last 12 months
- 2
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 12
| Code | Device | Class | Regulation | Premarket |
|---|---|---|---|---|
| HRX | CORUS Spinal SystemArthroscope | Class 2 | 21 CFR 888.1100 | K190201 |
| ODP | CAVUX® Cage-LXIntervertebral Fusion Device With Bone Graft, Cervical | Class 2 | 21 CFR 888.3080 | K122801 |
| OLO | CORUS Navigation System-GXOrthopedic Stereotaxic Instrument | Class 2 | 21 CFR 882.4560 | K251060 |
| OLO | CORUS Navigation Access SystemOrthopedic Stereotaxic Instrument | Class 2 | 21 CFR 882.4560 | K240625 |
| HWC | ALLY Bone ScrewScrew, Fixation, Bone | Class 2 | 21 CFR 888.3040 | K170698 |
| HST | PMT Cervical HarnessApparatus, Traction, Non-Powered | Class 1 | 21 CFR 888.5850 | — |
| GAD | DTRAX DiViNE SystemRetractor | Class 1 | 21 CFR 878.4800 | — |
| CCX | Cervical HarnessSupport, Patient PositionAdded Mar 24, 2026 | Class 1 | 21 CFR 868.6820 | — |
| MRW | CORUS PCSS 3D ImplantSystem, Facet Screw Spinal DeviceAdded May 15, 2026 | Unclassified | — | K253676 |
| MRW | CAVUX CAGE-EXPSystem, Facet Screw Spinal Device | Unclassified | — | K230297 |
| MRW | CORUS Posterior Cervical Stabilization System (PCSS)System, Facet Screw Spinal Device | Unclassified | — | K241035 |
| MRW | CAVUX Cage-LXSystem, Facet Screw Spinal Device | Unclassified | — | K230840 |
What changed
- Mar 24, 2026Listing added: CCX — Cervical Harness
- May 15, 2026Listing added: MRW — CORUS PCSS 3D Implant (K253676)