K260430
- 510(k) number
- K260430
- Device name
- Porcelain Etch Gel
- Applicant
- Belport Company, Inc., Gingi-Pak CA · US
- Product code
- KLE — Agent, Tooth Bonding, Resin
- Decision date
- 2026-04-10
- Date received
- 2026-02-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K260430
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.