Device Desk

Private service · Not FDA

FDA device establishment · Roaring Spring, PA

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-3030896267As of September 30, 2026

WellPact

Registration 3030896267FEI 3030896267Roaring Spring, PA

Owner/operator: NPC Inc.

  • 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
10
Added, last 12 months
10

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 10

CodeDeviceClassRegulationPremarket
OOXAutomated Occult Blood AnalyzerHematologyAdded Feb 9, 2026Class 221 CFR 864.6550K041408
QMABlood Collection Device For Cell-Free Nucleic AcidClinical ChemistryAdded Jan 9, 2026Class 221 CFR 862.1676K231776
FMKSingle Use Only Blood Lancet With An Integral Sharps Injury Prevention FeatureGeneral, Plastic SurgeryAdded Jan 9, 2026Class 221 CFR 878.4850K221126
GIMTubes, Vacuum Sample, With AnticoagulantClinical ChemistryAdded Jan 9, 2026Class 221 CFR 862.1675K231373
JKATubes, Vials, Systems, Serum Separators, Blood CollectionClinical ChemistryAdded Jan 9, 2026Class 221 CFR 862.1675K231373
FAQBag, Urine Collection, Leg, For External Use, SterileGastroenterology, UrologyAdded Feb 9, 2026Class 121 CFR 876.5250—
FMHContainer, Specimen, SterilePathologyAdded Feb 9, 2026Class 121 CFR 864.3250—
LRJDisinfectant, Medical DevicesGeneral HospitalAdded Jan 9, 2026Class 121 CFR 880.6890—
NABGauze / Sponge,Nonresorbable For External UseGeneral, Plastic SurgeryAdded Jan 9, 2026Class 121 CFR 878.4014—
KGXTape And Bandage, AdhesiveGeneral HospitalAdded Feb 9, 2026Class 121 CFR 880.5240—

What changed

  • Feb 9, 2026Listing added: OOX — Automated Occult Blood Analyzer (K041408)
  • Jan 9, 2026Listing added: QMA — Blood Collection Device For Cell-Free Nucleic Acid (K231776)
  • Jan 9, 2026Listing added: FMK — Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature (K221126)
  • Jan 9, 2026Listing added: GIM — Tubes, Vacuum Sample, With Anticoagulant (K231373)
  • Jan 9, 2026Listing added: JKA — Tubes, Vials, Systems, Serum Separators, Blood Collection (K231373)
  • Feb 9, 2026Listing added: FAQ — Bag, Urine Collection, Leg, For External Use, Sterile
  • Feb 9, 2026Listing added: FMH — Container, Specimen, Sterile
  • Jan 9, 2026Listing added: LRJ — Disinfectant, Medical Devices
  • Jan 9, 2026Listing added: NAB — Gauze / Sponge,Nonresorbable For External Use
  • Feb 9, 2026Listing added: KGX — Tape And Bandage, Adhesive
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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