Device Desk

Private service · Not FDA

FDA device establishment · South Setauket, NY

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-3031259044As of September 30, 2026

CARE LIVING DIAGNOSTICS INC

Registration 3031259044FEI 3031259044South Setauket, NY

Owner/operator: Care Living Diagnostics Inc

  • 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
12
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 12

CodeDeviceClassRegulationPremarket
CGAGlucose Oxidase, GlucoseClinical ChemistryClass 221 CFR 862.1345K052208
CAFNebulizer (Direct Patient Interface)AnesthesiologyAdded Nov 20, 2025Class 221 CFR 868.5630K230379
FMINeedle, Hypodermic, Single LumenGeneral HospitalAdded Dec 23, 2025Class 221 CFR 880.5570K221176
FMKSingle Use Only Blood Lancet With An Integral Sharps Injury Prevention FeatureGeneral, Plastic SurgeryClass 221 CFR 878.4850K221839
MEGSyringe, AntistickGeneral HospitalClass 221 CFR 880.5860K152808
FMFSyringe, PistonGeneral HospitalClass 221 CFR 880.5860K152808
IYOAstrasono Bladder Scanner A3Pro/A3Pro Lite/A3Essential/A5ProSystem, Imaging, Pulsed Echo, UltrasonicAdded May 25, 2026Class 221 CFR 892.1560K250331
DXNSystem, Measurement, Blood-Pressure, Non-InvasiveCardiovascularAdded Dec 23, 2025Class 221 CFR 870.1130K242721
NBWSystem, Test, Blood Glucose, Over The CounterClinical ChemistryClass 221 CFR 862.1345K052208
ITXAstrasono Bladder Scanner A3Pro/A3Pro Lite/A3Essential/A5ProTransducer, Ultrasonic, DiagnosticAdded May 25, 2026Class 221 CFR 892.1570K250331
CCQNebulizer, Medicinal, Non-Ventilatory (Atomizer)AnesthesiologyAdded Nov 20, 2025Class 121 CFR 868.5640—
JJXSingle (Specified) Analyte Controls (Assayed And Unassayed)Clinical ChemistryClass 121 CFR 862.1660K052208

What changed

  • Nov 20, 2025Listing added: CAF — Nebulizer (Direct Patient Interface) (K230379)
  • Dec 23, 2025Listing added: FMI — Needle, Hypodermic, Single Lumen (K221176)
  • May 25, 2026Listing added: IYO — Astrasono Bladder Scanner A3Pro/A3Pro Lite/A3Essential/A5Pro (K250331)
  • Dec 23, 2025Listing added: DXN — System, Measurement, Blood-Pressure, Non-Invasive (K242721)
  • May 25, 2026Listing added: ITX — Astrasono Bladder Scanner A3Pro/A3Pro Lite/A3Essential/A5Pro (K250331)
  • Nov 20, 2025Listing added: CCQ — Nebulizer, Medicinal, Non-Ventilatory (Atomizer)
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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