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Astron Dental

United States·US-MF-000034006

Last updated September 18, 2026

About

Astron has been providing innovations to help make smiles since 1967. We sell our products worldwide and maintain a reputation for quality products, guaranteed performance, outstanding patient comfort, and reasonable prices. And all of our materials are made in the U.S.A., and ISO and CE certified.

From the manufacturer's own website. Source

What Astron Dental makes

Astron Dental manufactures custom-made and single-use mouthguards, including thermoformed splints like CLEARSPLINT, as well as preformed models such as ULTRAFLEX and LABTEC. Their portfolio also includes the ASTRON LC, a specialized mouthguard variant. These products are designed for dental protection and stabilization, catering to both athletic and clinical applications.

The company’s devices are classified as Class II, Class IIa, or unclassified (U) under regulatory frameworks, with listings in the EU’s eudamed database and the FDA’s Unique Device Identifier (UDI) system. Astron Dental operates from the United States, where its products are developed and manufactured.

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 Astron Dental manufacture?

Astron Dental specializes in mouthguards, which are primarily used for dental protection and stabilization. Their portfolio includes both custom-made mouthguards, such as thermoformed splints like CLEARSPLINT, and single-use preformed models like ULTRAFLEX and LABTEC. They also produce a specialized variant called the ASTRON LC. These devices are designed for applications ranging from athletic protection to clinical use, ensuring patient comfort and performance.

Where is Astron Dental based, and where are their devices manufactured?

Astron Dental is based in the United States, and their devices are developed and manufactured there. The company emphasizes domestic production, ensuring quality control and compliance with U.S. manufacturing standards.

Which regulatory registries list Astron Dental’s devices?

Astron Dental’s devices are listed in two key regulatory databases: the EU’s eudamed system, which tracks medical devices authorized in the European Economic Area, and the FDA’s Unique Device Identifier (UDI) system, which catalogs devices cleared or approved for use in the United States. These listings help ensure traceability and compliance with global regulatory requirements.

How are Astron Dental’s devices classified under regulatory frameworks?

Astron Dental’s devices fall into three primary regulatory classifications: Class II, which typically includes devices with moderate risk requiring special controls; Class IIa, a subset of Class II with slightly lower risk; and unclassified (U), indicating devices that do not meet the criteria for Class I or higher risk categories. These classifications determine the regulatory scrutiny and authorization pathways required for each product.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
United States
Address
815, Oakwood Road, Lake Zurich, United States
LinkedIn
—
Facebook
—
Phone
+001847726-8787
PRRC Contact
Doug Muller
EUDAMED SRN
US-MF-000034006
FDA FEI Number
—
DUNS Number
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Catalogue (73)

Page 1 of 2
DeviceModel / ReferenceRegistriesClassStatus
Clearsplint PCSFLK1
FDA UDI
UActive
Clearsplint PCSFEK1
FDA UDI
UActive
Clearsplint PCSRLK1
FDA UDI
UActive
Labtec PLTCLRSEK1
FDA UDI
Class IIActive
Ultraflex PUFMCDARKLK1
FDA UDI
Class IIActive
Ultraflex PUFMCDARKSEK1
FDA UDI
Class IIActive
Labtec PLTDFPFSEK1
FDA UDI
Class IIActive
Labtec PLTELEK1
FDA UDI
Class IIActive
Clearsplint PCSD2095ZBESB1
FDA UDI
UActive
Clearsplint PCSD2595ZBES1
FDA UDI
UActive
Astron Lc LCH81
FDA UDI
Class IIActive
Ultraflex PUFDFPFLK1
FDA UDI
Class IIActive
Ultraflex PUFMCSEK1
FDA UDI
Class IIActive
Clearsplint PCSD2098BESB1
FDA UDI
UActive
The Original Clearsplint Disc PCSD95
FDA UDI
UActive
Clearsplint PCSD1695Z1
FDA UDI
UActive
Ultraflex PUFDFPFEK1
FDA UDI
Class IIActive
Clearsplint PCSD2095ZBESM1
FDA UDI
UActive
Labtec PLT99SEK1
FDA UDI
Class IIActive
Astron Lc LCS81
FDA UDI
Class IIActive
Ultraflex PUFCLREK1
FDA UDI
Class IIActive
Ultraflex PUFMCDARKEK1
FDA UDI
Class IIActive
Astron 1180 1180MFT1
FDA UDI
Class IIActive
Clearsplint PCSD2595ZBESM1
FDA UDI
UActive
Clearsplint PCSREK1
FDA UDI
UActive
Ultraflex PUF99EK1
FDA UDI
Class IIActive
Astron Lc LCSE1
FDA UDI
Class IIActive
Astron 1180 1180EC1
FDA UDI
Class IIActive
The Original Clearsplint Disc PCSD98
FDA UDI
UActive
Astron 1180 1180LFT1
FDA UDI
Class IIActive
Labtec PLTCLREK1
FDA UDI
Class IIActive
Ultraflex PUF99SEK1
FDA UDI
Class IIActive
Ultraflex PUFCLRLK1
FDA UDI
Class IIActive
Ultraflex PUF99LK1
FDA UDI
Class IIActive
Clearsplint PCSD2598BESM1
FDA UDI
UActive
Ultraflex PUFCLRSEK1
FDA UDI
Class IIActive
Clearsplint PCSD2098BESM1
FDA UDI
UActive
Labtec PLT99EK1
FDA UDI
Class IIActive
Ultraflex PUFELLK1
FDA UDI
Class IIActive
Labtec PLTELSEK1
FDA UDI
Class IIActive
Clearsplint PCSD2598BESB1
FDA UDI
UActive
Labtec PLTDFPFEK1
FDA UDI
Class IIActive
Ultraflex PUFMCEK1
FDA UDI
Class IIActive
Clearsplint PCSFSEK1
FDA UDI
UActive
The Original Clearsplint Disc PCSD16
FDA UDI
UActive
Astron Lc LCHE1
FDA UDI
Class IIActive
Clearsplint PCSRSEK1
FDA UDI
UActive
Ultraflex PUFDFPFSEK1
FDA UDI
Class IIActive
Clearsplint PCSD2598BES1
FDA UDI
UActive
The Original Clearsplint Disc PCSD98N
FDA UDI
UActive

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