BOCH GROUP LLC

FDA Device Registration & Listing · Burlington, CT, US · Registration 3010117482

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
3010117482
FEI Number
3010117482
Entity Name
BOCH GROUP LLC
City/State/Country
Burlington, CT, US
Establishment Address
12 Ventres Way, Burlington, CT 06013, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
BOCH Group LLC (Owner Number: 10043586)
Owner / Operator Contact Address
12 Ventres Way, Burlington, CT 06013, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Orthodontic Self Ligating Brackets

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EJF Bracket, Metal, Orthodontic Dental Class 1 872.5410 2013-03-01

Official Correspondent

Paul Blanchette

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BOCH Group LLC
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
K894358 Ormco Corp. LUMINA ORTHODONTIC BRACKET 1989-09-15
K925012 American Orthodontics PLASTIC CHAIN 1993-09-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010117482. Last updated year: 2026. Please use registration number 3010117482 when referencing this establishment in official correspondence.
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