Device Desk

Private service · Not FDA

FDA device establishment · Jacksonville, FL

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-1057946As of September 30, 2026

KLS-Martin L.P.

Registration 1057946FEI 1000525271Jacksonville, FL

Owner/operator: KLS Martin SE & Co. KG

  • 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
220
Added, last 12 months
12

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 220

CodeDeviceClassRegulationPremarket
JDQCerclage, FixationOrthopedicClass 221 CFR 888.3010K151983
JDQCerclage, FixationOrthopedicClass 221 CFR 888.3010K241018
JECComponent, Traction, InvasiveOrthopedicClass 221 CFR 888.3040K042066
PBJCranial Distraction SystemNeurologyClass 221 CFR 882.5330K163315
PBJCranial Distraction SystemNeurologyClass 221 CFR 882.5330K230211
PPTCranial Surgical Planning And Instrument GuidesNeurologyClass 221 CFR 882.4310K182889
PPTCranial Surgical Planning And Instrument GuidesNeurologyClass 221 CFR 882.4310K201052
DZJDriver, Wire, And Bone Drill, ManualDentalClass 221 CFR 872.4120K210731
DZJDriver, Wire, And Bone Drill, ManualDentalClass 221 CFR 872.4120K182789
DZJDriver, Wire, And Bone Drill, ManualDentalClass 221 CFR 872.4120K181241
MQNExternal Mandibular Fixator And/Or DistractorDentalClass 221 CFR 872.4760K032442
MQNExternal Mandibular Fixator And/Or DistractorDentalClass 221 CFR 872.4760K010139

and 208 more on your full dossier

What changed

  • Mar 11, 2026Listing added: GXP — Methyl Methacrylate For Cranioplasty (K252573)
  • Jan 13, 2026Listing added: PBF — Orthopaedic Surgical Planning And Instrument Guides (K250865)
  • Mar 11, 2026Listing added: JEY — Plate, Bone (K252573)
  • Mar 11, 2026Listing added: GXN — Plate, Cranioplasty, Preformed, Non-Alterable (K252573)
  • Mar 3, 2026Listing added: HRS — Plate, Fixation, Bone (K253660)
  • Mar 11, 2026Listing added: HRS — Plate, Fixation, Bone (K252573)
  • Jan 13, 2026Listing added: HRS — Plate, Fixation, Bone (K250865)
  • Mar 20, 2026Listing added: HRS — Plate, Fixation, Bone (K254162)
  • Jan 5, 2026Listing added: HRS — Plate, Fixation, Bone (K250988)
  • Mar 20, 2026Listing added: HWC — Screw, Fixation, Bone (K254162)
  • Jan 13, 2026Listing added: HWC — Screw, Fixation, Bone (K250865)
  • Mar 6, 2026Listing added: HRW — Dynamometer, Nonpowered
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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