Skip to content

FlexBracket 09.01.25.PCA.FB.LL5.022

by LightForce Orthodontics

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850079555761 UDI-DI Date14 Oct 2025ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
FlexBracket
Generic Name
Orthodontic bracket, ceramic
Model / Reference
09.01.25.PCA.FB.LL5.022
Primary DI / UDI-DI
00850079555761
510(k) Number
FDA Product Code
NJM
GMDN Term
Orthodontic bracket, ceramic
Device Class
Class II
Regulation Number
872.5470
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K232827)

Show all (12)

Other devices from LightForce Orthodontics

See all devices from LightForce Orthodontics →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No