# K912032: Silon (TM) Transparent Wound Dressing

- Pathway: 510(k) (Traditional)
- Applicant: Bio Med Sciences, Inc.
- Decided: Aug 20, 1991 after 104 days
- Product code: MGP (Dressing, Wound And Burn, Occlusive)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K990042: Silon Dual-Dress (1999), 0 descendants of its own
- K981665: Silon Topomat Corneal Topography Image Enhancement Device (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K912032
Methodology: https://510kreport.com/methodology