Lares Research 757 ProStyle SF Legacy 5
by Lares Research, Inc. 2 variants
Lares Research 757 ProStyle SF Legacy 5 (13142-236) is a Class I device made by Lares Research, Inc., cleared under FDA 510(k) K141221 on 28 Oct 2014 and listed in FDA GUDID since 7 Jun 2023 (UDI-DI D950131422360), 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 | NumberD950131422360 | Date7 Jun 2023 | StatusListed |
| United States | FDA 510(k)SESE | NumberK141221 | Date28 Oct 2014 | StatusActive |
Official records
- FDA 510(k) database K141221
Across registries
- FDA 510(k) K141221 decided 28 Oct 2014 Active
- FDA GUDID UDI-DI D950131422360 listed 7 Jun 2023 Listed
Timeline
- Cleared FDA 510(k) K141221
- Listed FDA GUDID D950131422360
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Lares Research
- Generic name
- Dental surgical power tool motorized handpiece/set, pneumatic
- Model / Ref / Catalog
- 757 ProStyle SF Legacy 5, 13142-236
- Primary DI / UDI-DI
- D950131422360
- 510(k) Number
- FDA product code
- EFB
- GMDN term
- Dental surgical power tool motorized handpiece/set, pneumatic
- Device class
- Class I
- Regulation number
- 872.4200
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under Dental surgical power tool motorized handpiece/set, pneumatic.