LAXMI DENTAL LAB USA INC.

FDA Device Registration & Listing · Kenilworth, NJ, US · Registration 3009432549

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
3009432549
FEI Number
3009432549
Entity Name
LAXMI DENTAL LAB USA INC.
City/State/Country
Kenilworth, NJ, US
Establishment Address
37 Market Street, Suite 202, Kenilworth, NJ 07033, US
Establishment Type(s)
Repack or Relabel Medical Device,Remanufacture Medical Device,Manufacture Medical Device
Owner / Operator
Laxmi Dental Lab USA Inc. (Owner Number: 10039895)
Owner / Operator Contact Address
37 Market Street, Suite 202, Kenilworth, NJ 07033, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Restoration, resin, crown and bridge Prosthesis, orthodontic Restoration, porcelain Dentures, partial

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NSN Restoration, Resin, Crown And Bridge Unknown Class N N/A 2013-08-27
NSR Prosthesis, Orthodontic Unknown Class N N/A 2013-08-27
NSP Restoration, Porcelain Unknown Class N N/A 2013-08-27
NSK Dentures, Partial Unknown Class N N/A 2013-08-27

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Laxmi Dental Lab USA Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009432549. Last updated year: 2026. Please use registration number 3009432549 when referencing this establishment in official correspondence.
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