FDA applicant
Kmb Medical Products Co.
FDA records 1 decision for Kmb Medical Products Co. (Hazelwood, MO) in 1988: 1 510(k) clearance. All are in product code FEG (Tube, Double Lumen For Intestinal…). 2 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Kmb Medical Products Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Kmb Medical Products Co. since 2007.
Recalls per year
1in 2025
2007high 1 (2024) · low 0 (2007)2026
Class I Class II/III not classified
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