Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Laborie Medical Technologies Corp.Labelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Laborie Medical Tech Corp. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Nov 29, 1999: UROSTYM BIOFEEDBACK AND STIMULATION ANAL/RECTAL PROBES.
| Nov 29, 1999 | UROSTYM BIOFEEDBACK AND STIMULATION ANAL/RECTAL PROBESK993721 · KPI | 510(k) clearances |
| Aug 5, 1999 | UROSTYM BIOFEEDBACK AND STIMULATION PROBESK990041 · KPI | 510(k) clearances |
| Jul 7, 1999 | VISER PENILE TUMESCENCE MONITORK991479 · LIL | 510(k) clearances |
| Jun 5, 1997 | ANO-RECTAL MANOMETRY OPTION, MODEL NUMBER UDS-ARMK963064 · FFX | 510(k) clearances |
| Mar 30, 1995 | CART, MODE NUMBER UDS-CARTK950016 · FEN | 510(k) clearances |
| May 10, 1994 | UORCAP,MODEL NUMBER UDS-UCAPK941105 · EXY | 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
