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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 7 of 37
DeviceModel / ReferenceRegistriesClassStatus
BioCosmetic® -217-1540
FDA UDI
Class IActive
Mini-Mono® -741-1463-010
FDA UDI
Class IActive
Mini-Sprint® -706-0920
FDA UDI
Class IActive
Mini-Mono® -740-0363-005
FDA UDI
Class IActive
Mini-Mono® -741-0371
FDA UDI
Class IActive
QuicKlear C733-0513
FDA UDI
Class IIActive
QuicKlear C706-1072
FDA UDI
Class IIActive
BioQuick® -738H1611-100
FDA UDI
Class IActive
BioQuick® -739-0513-005
FDA UDI
Class IActive
BioQuick® -738-1603-005
FDA UDI
Class IActive
BioQuick® -738H0511-005
FDA UDI
Class IActive
Forestanit® -213-8070
FDA UDI
Class IActive
QuicKlear C732-0401
FDA UDI
Class IIActive
BioQuick® -739-1613-100
FDA UDI
Class IActive
QuicKlear C706-1064
FDA UDI
Class IIActive
Mini-Sprint® -706-1059
FDA UDI
Class IActive
Mini-Mono® -775-2313-005
FDA UDI
Class IActive
Mini-Mono® N741-0321-010
FDA UDI
Class IActive
Mini-Mono® -775-3511
FDA UDI
Class IActive
QuicKlear C706-1080
FDA UDI
Class IIActive
Forestaflex® -253-4038
FDA UDI
Class IActive
Forestanit® -242-2080
FDA UDI
Class IActive
Mini-Mono® -723-0313-010
FDA UDI
Class IActive
QuicKlear® C706-1061
FDA UDI
Class IIActive
Mini-Mono® OA83-0301
FDA UDI
Class IActive
BioQuick® -739-1603
FDA UDI
Class IActive
QuicKlear® C706-1214
FDA UDI
Class IIActive
TruKlear® C706-2024
FDA UDI
Class IIActive
BioQuick® -706V0851
FDA UDI
Class IActive
BioQuick® -738H1403-010
FDA UDI
Class IActive
Mini-Mono® -776-2311-010
FDA UDI
Class IActive
BioQuick® -738-1501-005
FDA UDI
Class IActive
Sprint® -706-0649
FDA UDI
Class IActive
Mini-Mono® -775-2311-010
FDA UDI
Class IActive
Mini-Mono® -773-3203
FDA UDI
Class IActive
BioQuick® -738-1601-010
FDA UDI
Class IActive
Mini-Mono® N741-0321
FDA UDI
Class IActive
Mini-Mono® Brackets -706-0243
FDA UDI
Class IActive
BioQuick® -706-1215
FDA UDI
Class IActive
QuicKlear C706-1843
FDA UDI
Class IIActive
Mini-Mono® M775-3201
FDA UDI
Class IActive
Mini-Sprint® -706-0915
FDA UDI
Class IActive
BioQuick® -739H1511-005
FDA UDI
Class IActive
Mini-Mono® -775-3601-005
FDA UDI
Class IActive
Mini-Mono® -724-0313-005
FDA UDI
Class IActive
Mini-Mono® P775-3401
FDA UDI
Class IActive
Mini-Mono® -723-0303
FDA UDI
Class IActive
Mini Sprint ® -793-1611-010
FDA UDI
Class IActive
Mini-Mono® -775-2503-010
FDA UDI
Class IActive
BioQuick® -739-1611-010
FDA UDI
Class IActive

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