K932214Substantially Equivalent
Silon Silicone Gel Sheet
Bio Med Sciences, Inc., Bethlehem PA / Traditional, Substantially Equivalent
K932214 is the FDA 510(k) clearance record for SILON SILICONE GEL SHEET, a class I device, cleared for Bio Med Sciences, Inc. on under FDA product code MDA (Elastomer, Silicone, For Scar Management). FDA records list 10 510(k) clearances for Bio Med Sciences, Inc., from to . As of , FDA records show no recalls naming K932214.
Clearance record
- Decision date
- Received
- (244 days to decision)
- Product code
- MDA Elastomer, Silicone, For Scar Management
- Regulation
- 21 CFR 878.4025
- Device class
- Class I
- Review panel
- General, Plastic Surgery
- Applicant
- Bio Med Sciences, Inc. 115 Research Dr., Bethlehem PA
- 510(k) summary
- Statement
- Third party review
- No
Clearances, product code MDA
Trailing 12 monthsFDA records hold no clearances under product code MDA in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
