Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2020475

FEI Number

2020475

Entity Name

PROMA, INC.

City/State/Country

CARSON, CA, US

Establishment Address

730 EAST KINGSHILL PL., CARSON, CA 90746, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

PROMA, INC. (Owner Number: 2020475)

Owner / Operator Contact Address

730 EAST KINGSHILL PL., --, Carson, CA 90746, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DARAY BY PROMA

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EAZ	Light, Operating, Dental	Dental	Class 1	872.4630	1996-03-25

Official Correspondent

MIKE VILLANUEVA

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PROMA, INC.

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

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3015703934	MEDFRUITION ELECTRONICS TECHNOLOGY CO., LTD	Foshan City Guangdong, CN
3014766731	TAKARA BELMONT CORPORATION, OSAKA FACTORY	OSAKA, JP
3023443842	HENAN BAISTRA MEDICAL DEVICES LIMITED	Zhengzhou Henan, CN
2031508	TPC ADVANCED TECHNOLOGY, INC.	City Industry, CA, US
3022226	FOREST DENTAL EQUIPMENT	HILLSBORO, OR, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2020475. Last updated year: 2026. Please use registration number 2020475 when referencing this establishment in official correspondence.