Device Desk

Private service · Not FDA

FDA device establishment · Marlborough, MA

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-3012821221As of September 30, 2026

Global Life Sciences Solutions USA LLC

Registration 3012821221FEI 3012821221Marlborough, MA

Owner/operator: Global Life Sciences Solutions USA LLC

  • Complaint File Establishment per 21 CFR 820.198
  • Develop Specifications But Do Not Manufacture At This Facility

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
21
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 21

CodeDeviceClassRegulationPremarket
FYDLaparoShield Laparoscopic Smoke Filter; LaparoShield Plus Laparoscopic Smoke FilterApparatus, Exhaust, SurgicalClass 221 CFR 878.5070K992361
KSRMedtronic ATBAG1000; Medtronic ATBAG300; Medtronic ATBAG600Container, Empty, For Collection & Processing Of Blood & Blood ComponentsClass 221 CFR 864.9100BK840010
KSRFreezing Bag; Thermogenesis Freezing BagContainer, Empty, For Collection & Processing Of Blood & Blood ComponentsClass 221 CFR 864.9100BK980030
KSRThermogenesis Transfer/Freezing Bag Set; Transfer/Freezing Bag SetContainer, Empty, For Collection & Processing Of Blood & Blood ComponentsClass 221 CFR 864.9100BK980027
KSRCell Wash/Infusion Bag; Thermogenesis Cell Wash/Infusion BagContainer, Empty, For Collection & Processing Of Blood & Blood ComponentsClass 221 CFR 864.9100BK980038
OAOBriostor Transfer/Freezing Bag SetCord Blood Processing System And Storage ContainerClass 221 CFR 864.9900BK150314
CAHPall Corp Ultipor U55 Breathing Circuit Bacterial Filter and HMEFilter, Bacterial, Breathing-CircuitClass 221 CFR 868.5260K211286
CAHConserve Small Volume HME Filter; Ultipor 100 Breathing System Filter; Ultipor 100 Breathing System Filter with CO2 MoniFilter, Bacterial, Breathing-CircuitClass 221 CFR 868.5260K791307
CAHAnesthesia Breathing Circuit - Adult Kit 40 Coax; Anesthesia Breathing Circuit - Adult Kit 60 Coax; Anesthesia BreathingFilter, Bacterial, Breathing-CircuitClass 221 CFR 868.5260K013093
FPBGardian 25mm Syringe FilterFilter, Infusion LineClass 221 CFR 880.5440K802765
FPBTotal Nutrient Admixture Filter TNA; Total Nutrient Admixture Filter TNA1Filter, Infusion LineClass 221 CFR 880.5440K905794
FPBSUPOR; SUPOR AEFFilter, Infusion LineClass 221 CFR 880.5440K993379

and 9 more on your full dossier

What changed

  • Sep 3, 2026Listing added: FPB — Lipipor NLF1A NLF2A NLF2NTA TNA2A Infusion Filters (K261403)
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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