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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 3 of 37
DeviceModel / ReferenceRegistriesClassStatus
QuicKlear C706-1212
FDA UDI
Class IIActive
TruKlear C706-2030
FDA UDI
Class IIActive
TruKlear C713-0513
FDA UDI
Class IIActive
BioQuick® -738H0503-010
FDA UDI
Class IActive
Mini-Mono® -776-3411-100
FDA UDI
Class IActive
QuicKlear C706-0850
FDA UDI
Class IIActive
BioQuick® -706X0979
FDA UDI
Class IActive
Mini-Mono® -775-2503-100
FDA UDI
Class IActive
QuicKlear C732-1511
FDA UDI
Class IIActive
BioQuick® -739H0511-010
FDA UDI
Class IActive
BioQuick® -738H1601-100
FDA UDI
Class IActive
TruKlear® C706-2030
FDA UDI
Class IIActive
Mini Mono® -706-0293
FDA UDI
Class IActive
BioQuick® -738H1503-005
FDA UDI
Class IActive
Mini-Mono® Q776-3411-100
FDA UDI
Class IActive
Mini-Mono® -776-3401
FDA UDI
Class IActive
Mini Sprint ® -794-1601
FDA UDI
Class IActive
Mini-Mono® -740-1461
FDA UDI
Class IActive
QuicKlear C706-1076
FDA UDI
Class IIActive
Mini Sprint ® -794-1511-005
FDA UDI
Class IActive
Mini-Mono® -706-0277
FDA UDI
Class IActive
Mini-Mono® -775-3513
FDA UDI
Class IActive
BioQuick® -739H0311
FDA UDI
Class IActive
Mini-Sprint® -706-0912
FDA UDI
Class IActive
BioQuick® -731L0734-010
FDA UDI
Class IActive
Mini-Mono® Brackets Q714-1401-100
FDA UDI
Class IActive
Mini-Mono® -775-2501-010
FDA UDI
Class IActive
Mini-Mono® -706-0529
FDA UDI
Class IActive
QuicKlear C737-1511
FDA UDI
Class IIActive
BioQuick® -736-1203
FDA UDI
Class IActive
QuicKlear C732-1203
FDA UDI
Class IIActive
TruKlear C706-2000
FDA UDI
Class IIActive
BioCosmetic® -217-2040
FDA UDI
Class IActive
BioQuick® -706X0861
FDA UDI
Class IActive
QuicKlear C706-1045
FDA UDI
Class IIActive
TruKlear C715-0101
FDA UDI
Class IIActive
Forestaflex® -200-2355
FDA UDI
Class IActive
QuicKlear C706-6013
FDA UDI
Class IIActive
BioQuick® -733-0503-010
FDA UDI
Class IActive
BioQuick® -738-1603-100
FDA UDI
Class IActive
TruKlear C714-0311
FDA UDI
Class IIActive
Mini-Mono® -775-3201-005
FDA UDI
Class IActive
Mini Mono® -706-0296
FDA UDI
Class IActive
Mini-Mono® -706-0458
FDA UDI
Class IActive
Track A 1
FDA UDI
UActive
Mini Mono® M702-1203
FDA UDI
Class IActive
Nanda Braided Copper NiTi -200-2143
FDA UDI
Class IActive
Mini-Mono® -775-2213-100
FDA UDI
Class IActive
BioQuick® -739H1603-010
FDA UDI
Class IActive
QuicKlear C730-1613
FDA UDI
Class IIActive

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