Device Desk

Private service · Not FDA

FDA device establishment · Cheyenne, WY

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-3042708459As of September 30, 2026

NEOMEDICO, LLC

Registration 3042708459FEI 3042708459Cheyenne, WY

Owner/operator: Neomedico, 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
19
Added, last 12 months
19

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 19

CodeDeviceClassRegulationPremarket
MOZSYNVISC ONEAcid, Hyaluronic, IntraarticularAdded Jan 9, 2026Class 3—P940015
MOZDUROLANEAcid, Hyaluronic, IntraarticularAdded Jan 9, 2026Class 3—P170007
MOZSUPARTZAcid, Hyaluronic, IntraarticularAdded Jan 9, 2026Class 3—P980044
MOZHYALGANAcid, Hyaluronic, IntraarticularAdded Jan 9, 2026Class 3—P950027
MOZHYMOVISAcid, Hyaluronic, IntraarticularAdded Jan 9, 2026Class 3—P150010
MOZEUFLEXXAAcid, Hyaluronic, IntraarticularAdded Jan 9, 2026Class 3—P010029
MOZMONOVISCAcid, Hyaluronic, IntraarticularAdded Jan 9, 2026Class 3—P090031
MOZORTHOVISCAcid, Hyaluronic, IntraarticularAdded Jan 9, 2026Class 3—P030019
LMHSCULPTRA 2 vialsImplant, Dermal, For Aesthetic UseAdded Jan 9, 2026Class 3—P030050
LMHRESTYLANE 1ml with LidocaineImplant, Dermal, For Aesthetic UseAdded Jan 9, 2026Class 3—P140029
LMHBELOTERO BALANCEImplant, Dermal, For Aesthetic UseAdded Jan 9, 2026Class 3—P090016
LMHJUVEDERM VOLBELLA with LidocaineImplant, Dermal, For Aesthetic UseAdded Jan 9, 2026Class 3—P110033

and 7 more on your full dossier

What changed

  • Jan 9, 2026Listing added: MOZ — SYNVISC ONE (P940015)
  • Jan 9, 2026Listing added: MOZ — DUROLANE (P170007)
  • Jan 9, 2026Listing added: MOZ — SUPARTZ (P980044)
  • Jan 9, 2026Listing added: MOZ — HYALGAN (P950027)
  • Jan 9, 2026Listing added: MOZ — HYMOVIS (P150010)
  • Jan 9, 2026Listing added: MOZ — EUFLEXXA (P010029)
  • Jan 9, 2026Listing added: MOZ — MONOVISC (P090031)
  • Jan 9, 2026Listing added: MOZ — ORTHOVISC (P030019)
  • Jan 9, 2026Listing added: LMH — SCULPTRA 2 vials (P030050)
  • Jan 9, 2026Listing added: LMH — RESTYLANE 1ml with Lidocaine (P140029)
  • Jan 9, 2026Listing added: LMH — BELOTERO BALANCE (P090016)
  • Jan 9, 2026Listing added: LMH — JUVEDERM VOLBELLA with Lidocaine (P110033)
  • Jan 9, 2026Listing added: LMH — TEOSYAL RHA2 (P170002)
  • Jan 9, 2026Listing added: LMH — RADIESSE (+) 1.5ml with Lidocaine (P050052)
  • Jan 9, 2026Listing added: LMH — RADIESSE 3ml (P050037)
  • Jan 9, 2026Listing added: LMH — JUVEDERM ULTRA PLUS XC (P050047)
  • Jan 9, 2026Listing added: LMH — RESTYLANE EYELIGHT (P040024)
  • Jan 9, 2026Listing added: PKY — RESTYLANE EYELIGHT (P040024)
  • Jan 9, 2026Listing added: PKY — RADIESSE (+) 1.5ml with Lidocaine (P050052)
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

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Keep this desk: $249 a year

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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.