Dental Device Guide
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Registered with FDA

Head Dental Corp.

Irvine, CA, United States. Lists 4 dental device types with FDA across 1 registered establishment.

FDA owner/operator9051690Repacker / relabeler
Device types listed
4
Brands and models
4
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1United States

Devices listed with FDA

What Head Dental Corp. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Dental Air-Powered HandpieceEFB · Class 1Dental handpiecesLister
Handpiece, air-powered, dental
2023
Dental Contra- and Right-Angle Attachment HandpieceEGS · Class 1Dental handpiecesLister
Handpiece, air-powered, dental
2023
ArticulatorsEJP · Class 1Articulators & facebowsLister
PLIERS, ORTHODONTIC
2023
Orthodontic PlierJEX · Class 1Dental hand instrumentsLister
ORTHODONTIC PLIERS
2023

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

Also lists devices cleared under other names

Head Dental Corp. lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.

Original applicants: Nakamura Magnifier Co., Ltd. (1).

Decided510(k)DeviceApplicantDevice type
20 Mar 2008K073652ND LOW SPEED AIRMOTOR AND HANDPIECE, HIGHSPEED AIRTURBINE HANDPIECE, E-TYPE STRAIGHT NOSECONE AND CONTRA ANGLENakamura Magnifier Co., Ltd.EFB Dental Air-Powered Handpiece

Registered establishments

EstablishmentLocationWhat it does
HEAD DENTAL CORPORATIONFDA reg. 2087470Irvine, CA, United StatesRepacker / relabeler

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9051690). 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.