Device Desk

Private service · Not FDA

FDA device establishment · El Paso, 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-3017060084As of September 30, 2026

LARK INDUSTRIES

Registration 3017060084FEI 3017060084El Paso, TX

Owner/operator: Lark Industries

  • 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
77
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

  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 77

CodeDeviceClassRegulationPremarket
LPBBiosense Webster CablesCardiac Ablation Percutaneous CatheterClass 3—P990071
LPBCelsius Catheter, Celsius RMT Catheter, Celsius FLTR, Deflectable Diagnostic/Ablation Catheter, EZ Steer Catheter, EZ StCardiac Ablation Percutaneous CatheterClass 3—P950005
LPBTHERMOCOOL SMARTTOUCH Bi-Directional Navigation Catheter, Navigation CatheterCardiac Ablation Percutaneous CatheterClass 3—P040036
LPBEZ Steer Nav Catheter, NaviStar Catheter, NaviStar RMT Catheter, And Biosense Webster CablesCardiac Ablation Percutaneous CatheterClass 3—P990025
LPBBIOSENSE WEBSTER NAVISTAR/CELSIUS THERMO COOL DIAGNOSTIC/ABLATION DEFLECTABLE TIP CATHETERSCardiac Ablation Percutaneous CatheterClass 3—P030031
OAEBIOSENSE WEBSTER NAVISTAR/CELSIUS THERMO COOL DIAGNOSTIC/ABLATION DEFLECTABLE TIP CATHETERSCatheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial FibrillationClass 3—P030031
OAEBiosense Webster CablesCatheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial FibrillationClass 3—P990071
OADCelsius DS Catheter, EZ Steer DS Catheter, NaviStar DS Catheter, NaviStar RMT DS Catheter, EZ Steer DS NAV CatheterCatheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial FlutterClass 3—P010068
OADCelsius Catheter, Celsius RMT Catheter, Celsius FLTR, Deflectable Diagnostic/Ablation Catheter, EZ Steer Catheter, EZ StCatheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial FlutterClass 3—P950005
OADBiosense Webster CablesCatheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial FlutterClass 3—P990071
OADBIOSENSE WEBSTER NAVISTAR/CELSIUS THERMO COOL DIAGNOSTIC/ABLATION DEFLECTABLE TIP CATHETERSCatheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial FlutterClass 3—P030031
QZIBIOSENSE WEBSTER NAVISTAR/CELSIUS THERMO COOL DIAGNOSTIC/ABLATION DEFLECTABLE TIP CATHETERSPercutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible ElectroporationClass 3—P030031

and 65 more on your full dossier

What changed

  • Jul 6, 2026Listing added: MTD — OCTA LNG 48P 2-5-2-5-2 D-CURVE (K193237)
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.

Already a member? Sign in

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.

More device sites in Texas