THE LINDEN GROUP CORP.

FDA Device Registration & Listing · Cedar Knolls, NJ, US · Registration 3012336461

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
3012336461
FEI Number
3012336461
Entity Name
THE LINDEN GROUP CORP.
City/State/Country
Cedar Knolls, NJ, US
Establishment Address
2B Wing Dr, Cedar Knolls, NJ 07927, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Repack or Relabel Medical Device,Manufacture Medical Device
Owner / Operator
The Linden Group Corp. (Owner Number: 9092461)
Owner / Operator Contact Address
2B Wing Dr.,, Cedar Knolls, NJ 07927, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Optik View SC2784XX Series Optik View SC191XX Optik View SC551X Optik View SC5584XX Series Optik View SC242XX Optik View SC421X 42" Vividimage W HD Wall Display SC4284XX Series Optik View SC3184XX Series Optik View SC6584XX Series

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KQM Camera, Surgical And Accessories General, Plastic Surgery Class 1 878.4160 2015-12-29

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

The Linden Group Corp.
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 3012336461. Last updated year: 2026. Please use registration number 3012336461 when referencing this establishment in official correspondence.
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