Dental Delivery System
510(k) K896532
Dental Delivery System is a Class I device made by Dentech Corp., cleared under FDA 510(k) K896532 on 12 Feb 1990, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK896532 | Date12 Feb 1990 | StatusActive |
Official records
- FDA 510(k) database K896532
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- EIA
- Device class
- Class I
- Regulation
- 21 CFR Part 872.6640
- Advisory committee
- Dental
- FDA decision
- SESE Substantially Equivalent
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- STERISIL ANTIMICROBIAL TUBING AND BOTTLE by Sterisil
- INTEGO pro 6427277 by SIRONA Dental Systems GmbH
- ORALCAM by Charmac Group, Inc.
- LOGOS JUNIOR DENTAL CHAIR AND UNIT by Castellini S.P.A.
- PUMA DENTAL CHAIR AND UNIT by Castellini S.P.A.
- ENGLE DENTAL FAMILY OF DELIVERY SYSTEMS by Engle Dental Systems