TriRock Dental LLC

FDA Device Registration & Listing · Lakewood, NJ, US · Registration 3040602659

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
3040602659
FEI Number
3040602659
Entity Name
TriRock Dental LLC
City/State/Country
Lakewood, NJ, US
Establishment Address
1145 Towbin Ave, Lakewood, NJ 08701, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Repack or Relabel Medical Device
Owner / Operator
TriRock Dental LLC (Owner Number: 10094019)
Owner / Operator Contact Address
1145 Towbin Avenue, Lakewood, NJ 08701, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

TriRock Dental

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DZP Instrument, Diamond, Dental Dental Class 1 872.4535 2025-09-15

Official Correspondent

Diana Hernandez

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

TriRock Dental LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3040602659. Last updated year: 2026. Please use registration number 3040602659 when referencing this establishment in official correspondence.
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