Device Desk

Private service · Not FDA

FDA device establishment · Plano, TX

This page shows the yearly renewal for this site, from FDA’s public record.

Device Desk is a private service. We are not FDA. We never file or pay for you.

Renewal dossierDD-3016544248As of September 30, 2026

ANX ROBOTICA CORP.

Registration 3016544248FEI 3016544248Plano, TX

Owner/operator: AnX Robotica Corp.

  • 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.

90days left in the window

The 2026 window

  1. Oct 1Window opens91 days left
  2. Nov 3Where you stand58 days left
  3. Dec 1Our pay-by date30 days left
  4. Dec 15Two weeks left16 days left
  5. Dec 23Holiday week8 days left
  6. Dec 29Two days left2 days left
  7. Dec 31Window closes0 days left
an email on that date our pay-by date to December 31
FDA fee, FY2027
$13,785
Our pay-by suggestion
Dec 1
Listed devices
13
Added, last 12 months
5

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

  1. 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 process

  2. Wait 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 process

  3. Renew 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 listing

  4. Review 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 13

CodeDeviceClassRegulationPremarket
QZFProScan AI SoftwareGastrointestinal Capsule Endoscopy Analysis Software DeviceAdded Dec 29, 2025Class 221 CFR 876.1540DEN230027
NYVMotiliCap GI Monitoring SystemGastrointestinal Motility System, CapsuleAdded Dec 29, 2025Class 221 CFR 876.1725K250493
QKZNaviCam Capsule Endoscope System with NaviCam Stomach CapsuleMagnetically Maneuvered Capsule Endoscopy SystemClass 221 CFR 876.1310DEN190037
QKZNaviCam Xpress - 915 MHz CapsuleMagnetically Maneuvered Capsule Endoscopy SystemAdded Dec 29, 2025Class 221 CFR 876.1310K241934
QKZNaviCam Xpress - Lower Age Higher BMI IndicationMagnetically Maneuvered Capsule Endoscopy SystemAdded Dec 29, 2025Class 221 CFR 876.1310K231960
QKZNaviCam Capsule Endoscope System with NaviCam Stomach Capsule and NaviCam TetherMagnetically Maneuvered Capsule Endoscopy SystemClass 221 CFR 876.1310K221608
QKZNaviCam Xpress with GastroScanMagnetically Maneuvered Capsule Endoscopy SystemAdded Dec 29, 2025Class 221 CFR 876.1310K230694
QKZNaviCam Xpress Stomach Capsule Endoscope SystemMagnetically Maneuvered Capsule Endoscopy SystemClass 221 CFR 876.1310K203192
FFXIntraMarX Radiopaque MarkersSystem, Gastrointestinal Motility (Electrical)Class 221 CFR 876.1725K191087
FFXIntraMarX 3D Radiopaque MarkerSystem, Gastrointestinal Motility (Electrical)Class 221 CFR 876.1725K201106
NEZNaviCam Capsule/TetherSystem, Imaging, Gastrointestinal, Wireless, CapsuleClass 221 CFR 876.1300K233229
NEZNaviCam Small Bowel Capsule Endoscopy SystemSystem, Imaging, Gastrointestinal, Wireless, CapsuleClass 221 CFR 876.1300K221590

and 1 more on your full dossier

What changed

  • Dec 29, 2025Listing added: QZF — ProScan AI Software (DEN230027)
  • Dec 29, 2025Listing added: NYV — MotiliCap GI Monitoring System (K250493)
  • Dec 29, 2025Listing added: QKZ — NaviCam Xpress - 915 MHz Capsule (K241934)
  • Dec 29, 2025Listing added: QKZ — NaviCam Xpress - Lower Age Higher BMI Indication (K231960)
  • Dec 29, 2025Listing added: QKZ — NaviCam Xpress with GastroScan (K230694)
Data provided by the U.S. Food and Drug Administration (https://open.fda.gov). FDA does not endorse Device Desk.FDA’s own record is always the authority.

How we got this date

  1. FDA asks every device site to renew its registration each year.
  2. The renewal window runs from October 1, 2026 to December 31, 2026.
  3. A renewal in this window covers 2027.
  4. The rule is 21 CFR 807.22(b).

FDA’s record shows this registration runs through 2026.

We read this from FDA’s public record on September 30, 2026.

Read FDA’s page on registration

Watch for mail that looks like it is from FDA and asks you to pay a company. You pay FDA’s fee only in FDA’s own system.

Keep this desk: $249 a year

We keep this page current each week. We email you before each date in the window, and when FDA’s record shows you renewed.

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Renews each year until you cancel. Cancel any time from your account.

Is this right?

We copy this from FDA’s public record. FDA’s own record always wins. A listing missing here does not prove anything about FDA’s record.

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