510(k) Report

FDA applicant

National Patent Development Corp.

Mchenry, IL34 decisions1977–198570 recalls

FDA records 34 decisions for National Patent Development Corp. (Mchenry, IL) from 1977 to 1985: 34 510(k) clearances. Most are in product codes GAA (Needle, Aspiration And Injection, Disposable) and EIC (Syringe, Periodontic, Endodontic, Irrigating). 70 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided National Patent Development Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for National Patent Development Corp. since 2007.

Recalls per year

58in 2025

2008: 52009: 22021: 22023: 22025: 58
2007high 58 (2025) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — National Patent Development Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • GAANeedle, Aspiration And Injection, Disposable4decisions
  • EICSyringe, Periodontic, Endodontic, Irrigating4decisions
  • FPASet, Administration, Intravascular4decisions
  • FMFSyringe, Piston2decisions
  • KIFResin, Root Canal Filling2decisions
  • KMFBandage, Liquid2decisions

Also: EBF (2), KGX (2), FPB (1), EIL (1), KYX (1), BTO (1).

Who builds on its devices?

Later devices cite its devices 8 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K792227Multi-AD Fluid Dispensing SystemNational Patent Development Corp. · 19793cite it
  • K790062IV Administration Set with BackcheckNational Patent Development Corp. · 19792cite it
  • K780551I.V. Administration Set with Mini-SpikeNational Patent Development Corp. · 19781cites it
  • K790472Burron Vented NeedleNational Patent Development Corp. · 19791cites it
  • K790575Tube, Armored TrachealNational Patent Development Corp. · 19791cites it

What has FDA decided for it lately?

  • K843974Variable Temperature Cautery DeviceNational Patent Development Corp. · 1985
  • K832699Hydron Wound Dressing Fast Seat KitNational Patent Development Corp. · 1984
  • K822793Pio Root Canal IndicatorNational Patent Development Corp. · 1982
  • K820028Zeon Composite Resin Light Cure SysNational Patent Development Corp. · 1982
  • K820006Zeon Composite Resin SystemNational Patent Development Corp. · 1982
  • K811446Hydron Wound Dressing KitNational Patent Development Corp. · 1981
  • K801482Hydron Root Canal Filling MaterialNational Patent Development Corp. · 1980
  • K801484Root Canal Filling Applicator NeedlesNational Patent Development Corp. · 1980

All 34 as National Patent Development Corp. →

What has been recalled?

70 recalls linked to its devices; the latest:

  • K083723Anesthesia IV Set utilized in gravity IV administration sets and pump administration…Oct 29, 2025Class II
  • K781744Burette Set utilized in gravity IV administration sets and pump administration sets…Oct 29, 2025Class II
  • K083723Caresite utilized in gravity IV administration sets and pump administration sets…Oct 29, 2025Class II
  • K083723Anesthesia IV Set utilized in gravity IV administration sets and pump administration…Oct 29, 2025Class II
  • K083723Caresite utilized in gravity IV administration sets and pump administration sets…Oct 29, 2025Class II
  • K111016Extension Set utilized in gravity IV administration sets and pump administration sets…Oct 29, 2025Class II