Manufacturer registered with FDA

Proma, Inc.

Carson, CA, United States. Lists 2 dental device types with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator2020475Manufacturer

Device types listed: 2
Brands and models: 5
510(k) clearances: 11998–1998
Markets registered in: 1United States
Establishments: 1United States

510(k) clearances per year, 1990–2026

Devices listed with FDA

What Proma, Inc. currently lists, by FDA device type, with the brand and model names on the listing.

Device type	Category	Role	Brands and models	Listed since
Dental Operating LightEAZ · Class 1	Dental operating lights	Maker	DARAY BY PROMA	1996
Operative Dental UnitEIA · Class 1	Dental chairs & operative units	Maker	A SeriesAlliantDomainInception	2008

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

510(k) clearances

Clearances on which FDA names Proma, Inc. as the applicant.

Decided	510(k)	Device	Device type
3 Aug 1998	K980106	THE PROMA PERCEPTION, RESPONSE AND COMPASS SYSTEM AND ACCESSORIES	EIA Operative Dental Unit

Registered establishments

Establishment	Location	What it does
PROMA, INC.FDA reg. 2020475	CARSON, CA, United States	Manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 2020475). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.