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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 United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K141221

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD950131422360 UDI-DI Date7 Jun 2023ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Abbreviated NumberK141221 Date28 Oct 2014DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K141221 decided 28 Oct 2014 Active
  • FDA GUDID UDI-DI D950131422360 listed 7 Jun 2023 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K141221
  2. Listed FDA GUDID D950131422360

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

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

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Properties

  • Sterilise before use
  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)