Registered with FDA

MN Health Inc,

Chantilly, VA, United States. Lists 6 dental device types with FDA across 1 registered establishment.

FDA owner/operator10080654Repacker / relabeler
Device types listed
6
Brands and models
1
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1United States

Devices listed with FDA

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

Device typeCategoryRoleBrands and modelsListed since
Pulp TesterEAT · Class 2—Lister
raypulp
2025
Pit and Fissure Sealant and ConditionerEBC · Class 2Sealants & varnishesLister—2026
Resin Tooth Shade MaterialEBF · Class 2Dental compositesLister—2026
Air and/or Water Syringe UnitECB · Class 1Dental hand instrumentsLister—2026
X-Ray Film HolderEGZ · Class 1—Lister—2026
Resin ApplicatorKXR · Class 1—Lister—2025

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

MN Health Inc, 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: Medental Intl. (2).

Decided510(k)DeviceApplicantDevice type
14 Sep 1998K982191CHEMICAL CURE COMPOSITE WITH ENAMEL BONDMedental Intl.EBF Resin Tooth Shade Material
25 Nov 1997K973541MEDENTAL CHEMICAL CURING SEALANT PIT & FISSURE TINTEDMedental Intl.EBC Pit and Fissure Sealant and Conditioner

Registered establishments

EstablishmentLocationWhat it does
MN Health, IncFDA reg. 3018047916Chantilly, VA, United StatesRepacker / relabeler

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10080654). 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.