← Back to catalogue
ALL-ETCH, ALL- ETCH WITH BAC - Uni- Etch, Uni- Etch With Bac
FDA 510(k)Class II (US FDA 510(k))
510(k) K101485
by Bisco Inc.
Identifiers
- 510(k) Number
- K101485 FDA 510(k)
- FDA Product Code
- KLE FDA 510(k)
- Models / Variants
- All-Etch, All- Etch With Bac FDA 510(k)Uni- Etch, Uni- Etch With Bac FDA 510(k)Etch- 37, Etch- 37 With Bac FDA 510(k)Dark- Etch, Dark Etch (blue- E FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 872.3200 FDA 510(k)
- Regulation Number
- 872.3200 FDA 510(k)
- Advisory Committee
- Dental FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
ALL-ETCH, ALL- ETCH WITH BAC - Uni- Etch, Uni- Etch With Bac by Bisco Inc. — Class II — FDA_510K — listed in FDA 510(k) — 4 models
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K101485 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Bisco Inc.
- FDA Applicant
- Bisco, Inc.
Sources (1)
- FDA 510(k) K101485 24 fields · synced Jun 18, 2026