A-dec 532
by A-Dec, Inc.
A-dec 532 is a Class I device made by A-Dec, Inc., cleared under FDA 510(k) K032756 on 4 Dec 2003 and listed in FDA GUDID since 7 Nov 2022 (UDI-DI 10194665000011), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10194665000011 | Date7 Nov 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK032756 | Date4 Dec 2003 | StatusActive |
Official records
- AccessGUDID record 10194665000011
- FDA 510(k) database K032756
Across registries
- FDA 510(k) K032756 decided 4 Dec 2003 Active
- FDA GUDID UDI-DI 10194665000011 listed 7 Nov 2022 Listed
Timeline
- Cleared FDA 510(k) K032756
- Listed FDA GUDID 10194665000011
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- A-dec
- Generic name
- Dental delivery system
- Model / Ref / Catalog
- 532
- Primary DI / UDI-DI
- 10194665000011
- 510(k) Number
- FDA product code
- EIA
- GMDN term
- Dental delivery system
- Device class
- Class I
- Regulation number
- 872.6640
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Dental delivery system.
- OSSTEM IMPLANT CO., LTD. CHAIR BUSINESS K5 by OSSTEM IMPLANT Co., Ltd.
- Fi-G Z1211 by Guilin Woodpecker Medical Instrument Co., Ltd.
- PT-A Z121101 by Guilin Woodpecker Medical Instrument Co., Ltd.
- Dental treatment unit KLT-6220 by Foshan Roson Medical Instruments Co., Ltd
- NEO CART 0201 by Fimet Oy
- NEO CEILING 0203 by Fimet Oy
- CARVING 2025 by O.M.S. S.P.A. OFFICINE MECCANICHE SPECIALIZZATE
- Coltene Canalpro CL2 - by SAEYANG CO.,LTD.
- UM-1L 6680900 by CHANGZHOU SIFARY MEDICAL TECHNOLOGY CO., LTD.
- N2 (Continental Type) MC92-0008A by Megagen Implant Co., Ltd.