510(k) Report

FDA applicant

Nk Biotechnical Corp.

Minneapolis, MN2 decisions1997–19980 recalls

FDA records 2 decisions for Nk Biotechnical Corp. (Minneapolis, MN) from 1997 to 1998: 2 510(k) clearances. Most are in product codes HRW (Dynamometer, Nonpowered) and LBB (Dynamometer, Ac-Powered). No recall is linked to its devices.

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

FIG. A — Illustration, orthopedic panel, where it files most

How often FDA has decided Nk Biotechnical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nk Biotechnical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Nk Biotechnical 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?

  • HRWDynamometer, Nonpowered1decision
  • LBBDynamometer, Ac-Powered1decision

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K981730Digit-Grip with LCD, Model Number DGR 002Nk Biotechnical Corp. · 19981cites it

What has FDA decided for it lately?

  • K981730Digit-Grip with LCD, Model Number DGR 002Nk Biotechnical Corp. · 1998
  • K970870Digit-Grip with LCD (DGR002)Nk Biotechnical Corp. · 1997

All 2 as Nk Biotechnical Corp. →