STREAMLINE DENTAL PRODUCTS INC.

FDA Device Registration & Listing · New York, NY, US · Registration 3007028587

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
3007028587
FEI Number
3007028587
Entity Name
STREAMLINE DENTAL PRODUCTS INC.
City/State/Country
New York, NY, US
Establishment Address
237 W 37th St Fl 2, New York, NY 10018, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Streamline Dental Laboratory (Owner Number: 10025166)
Owner / Operator Contact Address
237 West 37th Street, 2nd Floor, New York, NY 10018, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

PARTIAL DENTURES FULL CAST BASE CAD/CAM RESTORATION PROVISIONAL ALL CERAMIC FULL DENTURE PFM GENERAL PFM NOBLE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NSK Dentures, Partial Unknown Class N N/A 2018-08-15
NSQ Restoration, Base Metal Unknown Class N N/A 2018-08-15
NOF System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations Dental Class 2 872.3661 2018-08-15
NSM Restoration, Resin Unknown Class N N/A 2018-08-15
ELW Material, Impression Dental Class 2 872.3660 2021-01-21
NSP Restoration, Porcelain Unknown Class N N/A 2018-08-15
NSL Dentures, Full Unknown Class N N/A 2018-08-15
NSO Restoration, Porcelain-Fused-To-Metal Unknown Class N N/A 2018-08-15
NSJ Restoration, Noble Metal Unknown Class N N/A 2018-08-15

Official Correspondent

Isaac Hakimi

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Streamline Dental Laboratory
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
K952614 Dentsply Intl. JELTRATE PLUS ANTIMICROBIAL IMPR. MATERIAL 1996-08-13

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3011275893 PROMAX DENTAL LABORATORY Zhuhai Guangdong, CN
3014270094 M/S LEIXIR RESOURCES PVT. LTD GURUGRAM Haryana, IN
3010594724 PREFERRED DENTAL LABORATORY, INC. Roseland, NJ, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007028587. Last updated year: 2026. Please use registration number 3007028587 when referencing this establishment in official correspondence.
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