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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 37 of 37
DeviceModel / ReferenceRegistriesClassStatus
QuicKlear C732-0511
FDA UDI
Class IIActive
QuicKlear C706-1051
FDA UDI
Class IIActive
BioQuick® -739H0501
FDA UDI
Class IActive
QuicKlear C731-1511
FDA UDI
Class IIActive
BioQuick® -739-1501
FDA UDI
Class IActive
Mini-Mono® -739-0323
FDA UDI
Class IActive
Mini-Sprint® -706-0926
FDA UDI
Class IActive
Sprint® -706-0639
FDA UDI
Class IActive
BioPassive® -706-1137
FDA UDI
Class IActive
BioQuick® -732E0713-005
FDA UDI
Class IActive
Mini-Mono® -706-0530
FDA UDI
Class IActive
Mini-Mono® -706-0209
FDA UDI
Class IActive
QuicKlear C739-0203
FDA UDI
Class IIActive
Mini Sprint ® -794-1613-010
FDA UDI
Class IActive
Mini-Mono® -775-3613
FDA UDI
Class IActive
BioQuick® -739-1501-010
FDA UDI
Class IActive
BioQuick® -739H1613-005
FDA UDI
Class IActive
TruKlear C713-0103
FDA UDI
Class IIActive
Mini-Mono® -706-0457
FDA UDI
Class IActive
BioQuick® -738H0503-100
FDA UDI
Class IActive
Track E 1
FDA UDI
UActive
QuicKlear C730-1513
FDA UDI
Class IIActive
QuicKlear C737-1513
FDA UDI
Class IIActive
Mini-Mono® -741-0381-010
FDA UDI
Class IActive
Mini-Mono® -776-3413-010
FDA UDI
Class IActive
BioQuick® -738H0311
FDA UDI
Class IActive
Mini Sprint® -779T0501-100
FDA UDI
Class IActive
Forestadent Brackets K924971
FDA 510(k)
Class IActive
Facebow K925240
FDA 510(k)
Class IIActive
Ortho Easy Pin K110275
FDA 510(k)
Class IIActive
Bernhard-Forster Gmbh Orthodontic Ceramic Brackets K090933
FDA 510(k)
Class IIActive

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