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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 2 of 37
DeviceModel / ReferenceRegistriesClassStatus
BioQuick® -706V0985
FDA UDI
Class IActive
BioQuick® -738H0313-005
FDA UDI
Class IActive
TruKlear® C706-2038
FDA UDI
Class IIActive
Mini-Mono® -775-3513-100
FDA UDI
Class IActive
BioQuick® -732E1713
FDA UDI
Class IActive
Mini-Mono® OA83-0101-100
FDA UDI
Class IActive
BioLingual® -270-0635
FDA UDI
Class IActive
Mini-Mono® Brackets -706-0238
FDA UDI
Class IActive
Mini-Mono® OA83-0513
FDA UDI
Class IActive
BioQuick® -732E0711-100
FDA UDI
Class IActive
Mini-Mono® -775-3613-100
FDA UDI
Class IActive
BioQuick® -706X0851
FDA UDI
Class IActive
BioQuick® -738-0503
FDA UDI
Class IActive
TruKlear C712-1203
FDA UDI
Class IIActive
TruKlear C706-2037
FDA UDI
Class IIActive
Mini-Mono® -776-3411-010
FDA UDI
Class IActive
QuicKlear C706-1052
FDA UDI
Class IIActive
BioQuick® -706X0856
FDA UDI
Class IActive
QuicKlear C732-0503
FDA UDI
Class IIActive
Forestanit® -213-3070
FDA UDI
Class IActive
BioQuick® -739-1503-010
FDA UDI
Class IActive
BioQuick® -739-1511
FDA UDI
Class IActive
Mini-Mono® -740-1203-100
FDA UDI
Class IActive
Mini-Mono® -775-3301-005
FDA UDI
Class IActive
BioQuick® -738H0313-010
FDA UDI
Class IActive
BioQuick® -738-1501-100
FDA UDI
Class IActive
Mini-Sprint® -706-1044
FDA UDI
Class IActive
BioQuick® -706V0850
FDA UDI
Class IActive
BioQuick® -733-0501-005
FDA UDI
Class IActive
BioQuick® -738H1601
FDA UDI
Class IActive
BioPassive® -706P0989
FDA UDI
Class IActive
BioQuick® -739-0503-100
FDA UDI
Class IActive
BioQuick® -732-0511-010
FDA UDI
Class IActive
BioQuick® -706E0872
FDA UDI
Class IActive
TruKlear C713-1511
FDA UDI
Class IIActive
TruKlear C714-1201
FDA UDI
Class IIActive
BioQuick® -738H1511
FDA UDI
Class IActive
Mini-Mono® NA84-0201-005
FDA UDI
Class IActive
Mini-Mono® Brackets -706-0235
FDA UDI
Class IActive
Mini-Sprint® -706-0922
FDA UDI
Class IActive
Mini-Mono® -706-0620
FDA UDI
Class IActive
Mini-Mono® -775-3413-010
FDA UDI
Class IActive
Mini-Mono® OA83-0203-005
FDA UDI
Class IActive
Mini-Sprint® -706-1030
FDA UDI
Class IActive
BioQuick® -733E0323-100
FDA UDI
Class IActive
QuicKlear C733-1611
FDA UDI
Class IIActive
BioQuick® -739H1613-100
FDA UDI
Class IActive
Mini-Mono® -740-1203-005
FDA UDI
Class IActive
QuicKlear C733-0413
FDA UDI
Class IIActive
Mini Sprint ® -794-1611
FDA UDI
Class IActive

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