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Sign in to claim this brandForestadent 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
- —
- Website
- forestadent.com
- —
- —
- [email protected]
- Phone
- +4972314590
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 316074384
Catalogue (1831)
Page 9 of 37| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| TruKlear | C712-1413 | FDA UDI | Class II | Active |
| Mini-Mono® | OA83-0201 | FDA UDI | Class I | Active |
| BioQuick® | -738H1411 | FDA UDI | Class I | Active |
| Mini-Mono® | -738-0323-100 | FDA UDI | Class I | Active |
| Sprint® | -706-0654 | FDA UDI | Class I | Active |
| BioQuick® | -739-0503-010 | FDA UDI | Class I | Active |
| QuicKlear® | C707-3023 | FDA UDI | Class II | Active |
| TruKlear | C712-0501 | FDA UDI | Class II | Active |
| BioQuick® | -739H1501 | FDA UDI | Class I | Active |
| BioQuick® | -733E0713-005 | FDA UDI | Class I | Active |
| TruKlear | C712-0201 | FDA UDI | Class II | Active |
| QuicKlear | C732-0101 | FDA UDI | Class II | Active |
| Mini-Mono® | N741-0321-005 | FDA UDI | Class I | Active |
| Mini-Mono® | -706-0580 | FDA UDI | Class I | Active |
| Mini Sprint ® | -794-1513-100 | FDA UDI | Class I | Active |
| QuicKlear | C706-6007 | FDA UDI | Class II | Active |
| QuicKlear | C739-1513 | FDA UDI | Class II | Active |
| Mini-Mono® | -706-0310 | FDA UDI | Class I | Active |
| Sprint® | -706-0659 | FDA UDI | Class I | Active |
| Mini-Mono® | N741-0333-005 | FDA UDI | Class I | Active |
| BioQuick® | -733-0501-010 | FDA UDI | Class I | Active |
| Mini-Mono® | OA83-0201-010 | FDA UDI | Class I | Active |
| Mini-Mono® | O740-0321 | FDA UDI | Class I | Active |
| Mini-Mono® | O740-0333 | FDA UDI | Class I | Active |
| BioQuick® | -733E0321-005 | FDA UDI | Class I | Active |
| Mini-Mono® | -706-0281 | FDA UDI | Class I | Active |
| QuicKlear | C732-0203 | FDA UDI | Class II | Active |
| BioQuick® | -738H1501 | FDA UDI | Class I | Active |
| Mini-Mono® | -723-0303-005 | FDA UDI | Class I | Active |
| Sprint® | -706-0665 | FDA UDI | Class I | Active |
| QuicKlear | C706-1091 | FDA UDI | Class II | Active |
| Mini-Mono® | -741-0371-005 | FDA UDI | Class I | Active |
| Mini-Mono® | -741-1461-100 | FDA UDI | Class I | Active |
| QuicKlear® | C706-1045 | FDA UDI | Class II | Active |
| BioQuick® | -739H0511 | FDA UDI | Class I | Active |
| BioQuick® | -739-0511-100 | FDA UDI | Class I | Active |
| BioQuick® | -738-1403-005 | FDA UDI | Class I | Active |
| TruKlear | C715-1613 | FDA UDI | Class II | Active |
| Mini-Mono® | M775-3501 | FDA UDI | Class I | Active |
| BioQuick® | -739H1401-005 | FDA UDI | Class I | Active |
| BioQuick® | -706H1217 | FDA UDI | Class I | Active |
| QuicKlear | C706-6017 | FDA UDI | Class II | Active |
| Mini Sprint® | -779T0503-100 | FDA UDI | Class I | Active |
| BioQuick® | -706H1201 | FDA UDI | Class I | Active |
| BioQuick® | -733E0323-005 | FDA UDI | Class I | Active |
| QuicKlear | C736-0101 | FDA UDI | Class II | Active |
| TruKlear | C715-0413 | FDA UDI | Class II | Active |
| QuicKlear | C706-1040 | FDA UDI | Class II | Active |
| BioQuick® | -739-1403-005 | FDA UDI | Class I | Active |
| Mini Sprint ® | -794-1501 | FDA UDI | Class I | Active |
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