# Laborie Medical Tech Corp.

- Location (FDA's records): Williston, VT
- FDA decisions: 6 (1994–1999): 6 510(k) clearances
- Names in FDA's records: Laborie Medical Tech Corp. (5); Laborie Medical Tech, Inc. (1)
- Product codes: KPI (2), LIL (1), FEN (1), EXY (1), FFX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K993721: Urostym Biofeedback and Stimulation Anal/Rectal Probes (Nov 29, 1999)
- K990041: Urostym Biofeedback and Stimulation Probes (Aug 5, 1999)
- K991479: Viser Penile Tumescence Monitor (Jul 7, 1999)
- K963064: Ano-Rectal Manometry Option, Model Number Uds-Arm (Jun 5, 1997)
- K950016: Cart, Mode Number Uds-Cart (Mar 30, 1995)
- K941105: Uorcap,Model Number Uds-Ucap (May 10, 1994)

Source page: https://510kreport.com/company/laborie-medical-tech