Device Desk

Private service · Not FDA

FDA device establishment · Athens, 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-1625425As of September 30, 2026

ARGON MEDICAL DEVICES INC.

Registration 1625425FEI 1625425ATHENS, TX

Owner/operator: ARGON MEDICAL DEVICES, INC

  • Develop Specifications But Do Not Manufacture At This Facility
  • Manufacture Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)
  • 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
157
Added, last 12 months
6

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 157

CodeDeviceClassRegulationPremarket
KOCArgon StopcockAccessories, Blood Circuit, HemodialysisClass 221 CFR 876.5820K770383
KNYWorker Guidewire AmplatzAccessories, Catheter, G-UClass 221 CFR 876.5130K991097
DTLArgon High Pressure LinesAdaptor, Stopcock, Manifold, Fitting, Cardiopulmonary BypassClass 221 CFR 870.4290K963749
DTLF/F Luer AdaptorAdaptor, Stopcock, Manifold, Fitting, Cardiopulmonary BypassClass 221 CFR 870.4290—
DTLArgon StopcockAdaptor, Stopcock, Manifold, Fitting, Cardiopulmonary BypassClass 221 CFR 870.4290K780271
DTLArgon High Pressure StopcockAdaptor, Stopcock, Manifold, Fitting, Cardiopulmonary BypassClass 221 CFR 870.4290K915301
DTLArgon Modified Disposable StopcockAdaptor, Stopcock, Manifold, Fitting, Cardiopulmonary BypassClass 221 CFR 870.4290K781579
OEQconvenience kitAngiography/Angioplasty KitClass 221 CFR 870.1650—
EXFD-Bag Drainage BagBag, Bile CollectingClass 221 CFR 876.5010K980005
FCGSABDBiopsy NeedleClass 221 CFR 876.1075K011270
LKFHSG Catheters, HSG Procedure TrayCannula, Manipulator/Injector, UterineClass 221 CFR 884.4530K000433
OEZKitsCardiovascular Procedure KitClass 221 CFR 870.1200—

and 145 more on your full dossier

What changed

  • Dec 9, 2025Listing added: DQO — Drakon and Sequre Microcatheters (K202797)
  • Dec 9, 2025Listing added: DQO — Drakon® and Sequre® Microcatheters (K231293)
  • Dec 9, 2025Listing added: DQO — Drakon® and Sequre® Microcatheters (K203487)
  • Dec 9, 2025Listing added: DQO — Drakon and Sequre Microcatheters (K173430)
  • Mar 16, 2026Listing added: DYB — V-Stick Vacular Access Set with Talwire (K253741)
  • Mar 16, 2026Listing added: DQX — V-Stick Vacular Access Set with Talwire (K253741)
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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