Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2247044

FEI Number

1000122242

Entity Name

HIGH POINT PRECISION PRODUCTS

City/State/Country

SUSSEX, NJ, US

Establishment Address

1 FIRST ST., SUSSEX, NJ 07461, US

Establishment Type(s)

Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

HIGH POINT PRECISION PRODUCTS (Owner Number: 9001241)

Owner / Operator Contact Address

1 FIRST ST., Sussex, NJ 07461, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Root Canal Post

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ELR	Post, Root Canal	Dental	Class 1	872.3810	2013-09-04

Official Correspondent

Marie O Connor

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

HIGH POINT PRECISION PRODUCTS

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3023852420	Hipp Medical AG	Renquishausen Baden-Wurttemberg, DE
2244812	DMG America LLC	ENGLEWOOD, NJ, US
3013557562	CBR ENTERPRISE LIMITED	Hong Kong, HK
3043648115	DEBO MEDICAL TECHNOLOGY (SHIJIAZHUANG) CO., LTD.	Shijiazhuang Hebei, CN
3011713204	Henan Lusterdent Medical Instrument Co.,Ltd	Zhengzhou Henan, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2247044. Last updated year: 2026. Please use registration number 2247044 when referencing this establishment in official correspondence.