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 Medical Device Inspection Co., Inc. with 30 510(k) clearances. The most recent is a 510(k) clearance dated Aug 4, 1995: J & J I-330 SERIES PHYSIOLOGICAL MONITORING & BIOFEEDBACK INSTUMENT AND USE SOFTWARE APP….
| Aug 4, 1995 | J & J I-330 SERIES PHYSIOLOGICAL MONITORING & BIOFEEDBACK INSTUMENT AND USE SOFTWARE APPLICATIONSK945826 · HCC | 510(k) clearances |
| Jan 11, 1994 | JARIT SURGICAL INSTRUMENTSK932072 · HET | 510(k) clearances |
| Dec 21, 1993 | THERA-TURN CM-1000 MATTRESS OVERLAY SYSTEMK931594 · IOQ | 510(k) clearances |
| Nov 5, 1993 | POWERMATIC MAT PLATFORMK933578 · INQ | 510(k) clearances |
| Nov 5, 1993 | POWER WORK TABLEK933580 · INQ | 510(k) clearances |
| Nov 5, 1993 | POWERMATIC TREATMENT TABLEK933581 · INQ | 510(k) clearances |
| Sep 30, 1993 | POWERMATIC EXAMINATION TABLEK933577 · INQ | 510(k) clearances |
| May 26, 1992 | SHOWER CHAIRSK922045 · INM | 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
