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Forestadent Bernhard Förster GmbH

US

Last updated May 24, 2026

What Forestadent Bernhard Förster GmbH makes

Forestadent Bernhard Förster GmbH manufactures orthodontic brackets in metal and ceramic, along with orthodontic archwires and wires for dental alignment. Their portfolio also includes thermoplastic materials for dental appliance fabrication and reusable surgical screwdrivers. Additionally, they produce liquid chromatography kits for detecting organic solvent metabolites as an in vitro diagnostic test.

The company’s devices are classified as Class I, Class II, or unclassified (U) under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Forestadent Bernhard Förster GmbH manufacture?

Forestadent Bernhard Förster GmbH primarily manufactures orthodontic devices, including metal and ceramic brackets, orthodontic archwires, and wires used for dental alignment. Their portfolio also includes thermoplastic materials for fabricating dental appliances and reusable surgical screwdrivers. Additionally, they produce in vitro diagnostic (IVD) kits for liquid chromatography used to detect organic solvent metabolites.

Where is Forestadent Bernhard Förster GmbH based?

Forestadent Bernhard Förster GmbH is based in the United States. The company’s location is relevant for regulatory compliance and device listing purposes, particularly under FDA jurisdiction.

Which regulatory registries list Forestadent Bernhard Förster GmbH’s devices?

Forestadent Bernhard Förster GmbH’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for orthodontic, surgical, and diagnostic devices under FDA oversight.

How are Forestadent Bernhard Förster GmbH’s devices classified under FDA regulations?

Forestadent Bernhard Förster GmbH’s devices fall into three classification categories: Class I (generally low-risk), Class II (moderate-risk requiring special controls), or unclassified (U). Classification depends on factors like intended use, risk level, and regulatory pathways, with orthodontic brackets and wires typically falling into Class I or II.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
+4972314590
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
316074384

Catalogue (1831)

Page 5 of 37
DeviceModel / ReferenceRegistriesClassStatus
TruKlear C706-2040
FDA UDI
Class IIActive
OrthoEasy® 1199-0015
FDA UDI
Class IActive
BioQuick® -707-5522
FDA UDI
Class IActive
Mini-Sprint® -706-0932
FDA UDI
Class IActive
Mini-Mono® -773-2503-010
FDA UDI
Class IActive
BioQuick® -738-1503-010
FDA UDI
Class IActive
Mini-Mono® -706-0630
FDA UDI
Class IActive
Mini-Mono® M775-3201-005
FDA UDI
Class IActive
BioQuick® -732E0321-010
FDA UDI
Class IActive
QuicKlear C736-0501
FDA UDI
Class IIActive
QuicKlear® C707-3020
FDA UDI
Class IIActive
Mini-Mono® -775-3403-010
FDA UDI
Class IActive
BioQuick® -739-1403-100
FDA UDI
Class IActive
BioQuick® -732E1613-100
FDA UDI
Class IActive
TruKlear C713-0203
FDA UDI
Class IIActive
Mini-Sprint® -706-1049
FDA UDI
Class IActive
TruKlear C715-0313
FDA UDI
Class IIActive
BioQuick® -733E0313-100
FDA UDI
Class IActive
BioQuick® -738H0511-100
FDA UDI
Class IActive
Mini-Mono® L775-2503-100
FDA UDI
Class IActive
QuicKlear C738-1301
FDA UDI
Class IIActive
Mini-Mono® OA83-0103-005
FDA UDI
Class IActive
Mini-Mono® -706-0634
FDA UDI
Class IActive
Mini Sprint® -780T0513
FDA UDI
Class IActive
Mini-Mono® OA83-0103
FDA UDI
Class IActive
Mini-Mono® -774-2303-010
FDA UDI
Class IActive
Mini-Mono® -775-3411-100
FDA UDI
Class IActive
Mini-Mono® -706-0614
FDA UDI
Class IActive
BioQuick® -738-0513-010
FDA UDI
Class IActive
Mini-Mono® -776-2311-100
FDA UDI
Class IActive
BioQuick® -739H1603
FDA UDI
Class IActive
TruKlear® C707-3015
FDA UDI
Class IIActive
BioQuick® -733E0321-100
FDA UDI
Class IActive
Mini Sprint ® -794-1603-005
FDA UDI
Class IActive
BioQuick® -732-0513-005
FDA UDI
Class IActive
BioQuick® -706H1215
FDA UDI
Class IActive
BioLingual® -270-0130
FDA UDI
Class IActive
Mini-Mono® -775-3503-005
FDA UDI
Class IActive
Mini-Mono® -741-0371-010
FDA UDI
Class IActive
Mini-Mono® -740-1461-010
FDA UDI
Class IActive
QuicKlear® C706H1214
FDA UDI
Class IIActive
BioQuick® -739H1613-010
FDA UDI
Class IActive
Forestanit® -212-2070
FDA UDI
Class IActive
Mini-Mono® -706-0559
FDA UDI
Class IActive
Mini-Mono® -740-1201-100
FDA UDI
Class IActive
QuicKlear C706-1073
FDA UDI
Class IIActive
QuicKlear C738-0101
FDA UDI
Class IIActive
Mini-Mono® NA84-0513
FDA UDI
Class IActive
Mini-Mono® -776-2303-100
FDA UDI
Class IActive
Mini Sprint ® -793-1511-005
FDA UDI
Class IActive

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