Forest 2520C
Forest 2520C is a Class I device made by Ls Enterprises, Inc., cleared under FDA 510(k) K173608 on 17 Aug 2018 and listed in FDA GUDID since 8 Dec 2022 (UDI-DI D0692520C0), 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 | GUDID listing | NumberD0692520C0 | Date8 Dec 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK173608 | Date17 Aug 2018 | StatusActive |
Official records
- FDA 510(k) database K173608
Across registries
- FDA 510(k) K173608 decided 17 Aug 2018 Active
- FDA GUDID UDI-DI D0692520C0 listed 8 Dec 2022 Listed
Timeline
- Cleared FDA 510(k) K173608
- Listed FDA GUDID D0692520C0
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Forest
- Generic name
- Dental delivery system
- Model / reference
- 2520C
- Primary DI / UDI-DI
- D0692520C0
- 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.
- 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
- CHIROMEGA s.r.o. CHIROMEGA 654 SOLO by CHIROMEGA
- NEO 0200 by Fimet Oy
- CLESTA eIII CHAIR AC-CL3-C230CET by Takara Belmont Corporation