Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list NK Biotechnical Engineering Co. with 15 510(k) clearances. The most recent is a 510(k) clearance dated Aug 11, 1994: NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001.
| Aug 11, 1994 | NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001K934368 · LLN | 510(k) clearances |
| May 12, 1993 | NK GRASP SENSOR, MODEL GA002K923965 · LBB | 510(k) clearances |
| May 12, 1993 | NK GRASP SENSOR, MODEL GA001K923964 · LBB | 510(k) clearances |
| Mar 31, 1993 | NK DIGI-GRIP SENSOR, MODEL DGR001K923963 · LBB | 510(k) clearances |
| Jul 14, 1992 | NK DYNA-GRIP SENSOR, MODEL DG001K921268 · LBB | 510(k) clearances |
| Jul 14, 1992 | NK MEDICAL MICROMETER, MODEL MC001K921266 · KTZ | 510(k) clearances |
| Dec 9, 1991 | RANGE OF MOTION SENSOR, MODEL RM001K914060 · KQX | 510(k) clearances |
| Dec 9, 1991 | NK DEVIATION SENSOR, MODEL DV001K914059 · LBB | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
