Beaucor
510(k) K812551
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK812551 | Date23 Sep 1981 | StatusActive |
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- EBF
- Device Class
- Class II
- Regulation
- 21 CFR Part 872.3690
- Advisory Committee
- Dental
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 27 Sep 2026
Beaucor is a dental chair designed for use in dental settings. It serves as a specialized seating system to support patients during dental procedures.
This device is manufactured by Sci-Pharm, Inc. and has received FDA 510(k) clearance. It is identified by the product code EBF and reference number K812551.
Other devices from Sci-Pharm, Inc.
Questions
AI-generated answers, 27 Sep 2026
What is the primary purpose of the Beaucor dental chair?
The Beaucor is a specialized seating system engineered specifically for use in dental settings to provide stable and ergonomic support for patients throughout various dental procedures.
Who is the manufacturer of the Beaucor dental chair?
The Beaucor dental chair is manufactured by Sci-Pharm, Inc., located in McHenry, Illinois.
What is the regulatory status of the Beaucor dental chair?
The Beaucor dental chair has received FDA 510(k) clearance under reference number K812551. This indicates that the device has been determined to be substantially equivalent to legally marketed predicate devices.