LightForce Orthodontics

FDA Device Registration & Listing · Wilmington, MA, US · Registration 3027460334

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3027460334
FEI Number
3027460334
Entity Name
LightForce Orthodontics
City/State/Country
Wilmington, MA, US
Establishment Address
400 Research Dr., Ste 125, Wilmington, MA 01887, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
LightForce Orthodontics, Inc (Owner Number: 10059693)
Owner / Operator Contact Address
400 Research Drive, Suite 125, Wilmington, MA 01887, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K183542
PMA Number
N/A

All Registered Proprietary Names

LightForce Orthodontic System LightForce Orthodontic System LightForce Orthodontic System LightForce Orthodontic System Signature Orthodontics

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PNN Orthodontic Software Dental Class 2 872.5470 2024-05-08
NJM Bracket, Ceramic, Orthodontic Dental Class 2 872.5470 2024-05-08
NJM Bracket, Ceramic, Orthodontic Dental Class 2 872.5470 2022-10-16
PNN Orthodontic Software Dental Class 2 872.5470 2022-10-16
NJM Bracket, Ceramic, Orthodontic Dental Class 2 872.5470 2022-10-16
NJM Bracket, Ceramic, Orthodontic Dental Class 2 872.5470 2019-02-12

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LightForce Orthodontics, Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K180404 3M Healthcare 3M Clarity Ultra Self-Ligating Brackets and Adhesive Coated Appliance System 2018-03-16

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027460334. Last updated year: 2026. Please use registration number 3027460334 when referencing this establishment in official correspondence.
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