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 Kent Design & Manufacturing, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Aug 20, 1986: PORTABLE ISOKINETICS 3004 KNEE UNIT.
| Aug 20, 1986 | PORTABLE ISOKINETICS 3004 KNEE UNITK862996 · IKK | 510(k) clearances |
| Aug 20, 1986 | PORTABLE ISOKINETICS 3007 BACK/ABDOMEN UNITK862998 · IKK | 510(k) clearances |
| Aug 20, 1986 | PORTABLE ISOKINETICS 3002 ISO KANE IIK862994 · IKK | 510(k) clearances |
| Aug 20, 1986 | PORTABLE ISOKINETICS 3001 WRIST/ANKLE UNITK862993 · IKK | 510(k) clearances |
| Aug 20, 1986 | PORTABLE ISOKINETICS 3005 HIP UNITK862997 · IKK | 510(k) clearances |
| Aug 20, 1986 | PORTABLE ISOKINETICS 3003 SHOULDER UNITK862995 · IKK | 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
