Registered with FDA

Forestadent Usa

Earth City, MO, United States. Lists 10 dental device types with FDA across 1 registered establishment.

FDA owner/operator9074785Repacker / relabeler
Device types listed
10
Brands and models
49
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1United States

Devices listed with FDA

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

Device typeCategoryRoleBrands and modelsListed since
Orthodontic Screw Expansion RetainerDYJ · Class 1Retainers, expanders & headgearLister
RETAINERSCREW EXPANSION
2005
Orthodontic WireDZC · Class 1Orthodontic wires & bandsLister
WIRE
2005
Orthodontic TubeDZD · Class 1Orthodontic wires & bandsLister
AlexanderAndrewsAspireBioQuickGlamHilgersMicro SprintMini SprintRickettsSmile Rx
5 more
SprintStandard EdgewiseVertical Slot2D Lingual3D Lingual
2005
Orthodontic Elastic BandECI · Class 1Orthodontic wires & bandsLister
BAND
2005
Orthodontic Preformed BandECM · Class 1Orthodontic wires & bandsLister
BAND
2005
Orthodontic Wire ClampECN · Class 1—Lister
CLAMP WIRE
2005
Orthodontic SpringECO · Class 1Orthodontic wires & bandsLister
SPRING
2005
Preformed ClaspEHP · Class 1—Lister
CLASP
2005
Orthodontic Metal BracketEJF · Class 1Orthodontic bracketsLister
Alexander SAspire CeramicAspire PlusBioPassiveBioQuickGlamHilgers SMBT S2Micro SprintMini Ants
13 more
Mini SprintQuicKlearRicketts NRicketts SRoth NRoth N Offset Bi'sRoth N Vertical slotSmile RxSprintStandard Edgewise NStandard Edgewise S2D Lingual2D Plus Lingual
2005
Orthodontic PlierJEX · Class 1Dental hand instrumentsLister
Classic InstrumentsExpression InstrumentsPremier Instruments
2005

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

Registered establishments

EstablishmentLocationWhat it does
FORESTADENT USAFDA reg. 3005014825Earth City, MO, United StatesRepacker / relabeler

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9074785). 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.