A-dec 333pro
by A-Dec, Inc.
A-dec 333pro is a Class I device made by A-Dec, Inc., cleared under FDA 510(k) K213932 on 2 Mar 2022 and listed in FDA GUDID since 10 May 2023 (UDI-DI 10194665005863), 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 | Number10194665005863 | Date10 May 2023 | StatusListed |
| United States | FDA 510(k)SESE | NumberK213932 | Date2 Mar 2022 | StatusActive |
Official records
- AccessGUDID record 10194665005863
- FDA 510(k) database K213932
Across registries
- FDA 510(k) K213932 decided 2 Mar 2022 Active
- FDA GUDID UDI-DI 10194665005863 listed 10 May 2023 Listed
Timeline
- Cleared FDA 510(k) K213932
- Listed FDA GUDID 10194665005863
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- Withdrawn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
- 333pro
- Primary DI / UDI-DI
- 10194665005863
- 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.
- UM-1L 6680900 by CHANGZHOU SIFARY MEDICAL TECHNOLOGY CO., LTD.
- N2 (Continental Type) MC92-0008A by Megagen Implant Co., Ltd.
- E-connect S 6080051 by CHANGZHOU SIFARY MEDICAL TECHNOLOGY CO., LTD.
- Fi-E (EDGEFLOW) Z1211 by Guilin Woodpecker Medical Instrument Co., Ltd.
- EndoMaster by Shanwei Perfect Medical Instruments Co., Ltd.
- Planmeca Pro50 30045357 by Planmeca Oy
- MASTERsurg LUX Wireless 1.009.1200 NA by KaVo Dental GmbH
- INTEGO pro 6427277 by SIRONA Dental Systems GmbH
- Dental controllers for contra angle handpieces - by SAEYANG CO.,LTD.
- F1 Arcus 0140 by Fimet Oy