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Sign in to claim this brandBISCO INC.
US
Last updated May 24, 2026
What BISCO INC. makes
Bisco Inc. manufactures dental materials and accessories for restorative procedures, including composite resins, bonding agents, and dental cements. Their portfolio includes trial pastes for temporary restorations, single-use application tools, and specialized mixing nozzles for precise material dispensing. The company also produces dental etching solutions, priming agents for prostheses, and resin-based modeling materials for dental applications.
Bisco Inc.’s products are regulated under the FDA’s UDI system, with devices classified as either Class I or Class II. These materials are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. medical device regulations. The company operates from 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 Bisco Inc. manufacture?
Bisco Inc. specializes in dental materials and accessories primarily used in restorative procedures. Their portfolio includes dental composite resins for fillings, bonding agents and sets for tooth preparation, dental etching solutions to prepare tooth surfaces, trial pastes for temporary restorations, and specialized tools like single-use application nozzles and cannulas for precise material dispensing. These products are designed to support procedures such as bonding, cementation, and prosthesis preparation in dental settings.
Where is Bisco Inc. based, and how does that affect its regulatory compliance?
Bisco Inc. is based in the United States, which means its devices are subject to U.S. regulatory requirements, including those managed by the FDA. Since the company’s products are listed in the FDA’s Unique Device Identifier (UDI) database, they comply with U.S. traceability and identification standards. The FDA classifies these devices as either Class I or Class II, depending on their risk level and intended use, ensuring they meet applicable regulatory criteria for safety and effectiveness.
Which regulatory registries or databases list Bisco Inc.’s devices?
Bisco Inc.’s devices are included in the FDA’s Unique Device Identifier (UDI) database. The UDI system assigns a standardized identifier to each device, enabling better tracking, traceability, and compliance monitoring in the U.S. market. This listing helps ensure transparency and regulatory oversight of the company’s dental materials and accessories.
How are Bisco Inc.’s devices classified under U.S. regulations?
Bisco Inc.’s devices are classified under the FDA’s medical device classification system as either Class I or Class II. Class I devices generally pose minimal risk and may require general controls for regulation, while Class II devices involve a higher level of risk and require special controls to ensure their safety and performance. The classification depends on factors like the device’s intended use, potential risks, and the procedures it supports in dental care.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- bisco.com
- —
- —
- [email protected]
- Phone
- +1(847)534-6000
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 053529939
Catalogue (1223)
Page 25 of 25| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bisco Porcelain Repair Kit | K874557 | FDA 510(k) | Class II | Active |
| Bisco Universal Hybrid Composite | K934247 | FDA 510(k) | Class II | Active |
| Bisfil-M(light Curable Anterior Composite) | K853001 | FDA 510(k) | Class II | Active |
| All-Etch, All- Etch With Bac; Uni- Etch, Uni- Etch With Bac; Etch- 37, Etch- 37 With Bac; Dark- Etch, Dark Etch (blue- E | K101485 | FDA 510(k) | Class II | Active |
| Ecliptomer | K945604 | FDA 510(k) | Class II | Active |
| Renew Ls-1 | K003317 | FDA 510(k) | Class II | Active |
| HAPI Seal | K162598 | FDA 510(k) | Class II | Active |
| Tescera Glazing Resin, Model T-1804, Biscover Xt, Model G-93220p | K024046 | FDA 510(k) | Class II | Active |
| Biscolor | K875256 | FDA 510(k) | Class II | Active |
| Bisco Cavity Cleanser | K915668 | FDA 510(k) | Class II | Active |
| Total Cure | K010196 | FDA 510(k) | Class II | Active |
| Biscem Gi | K032597 | FDA 510(k) | Class II | Active |
| Renew | K982729 | FDA 510(k) | Class II | Active |
| Dreambond | K112118 | FDA 510(k) | Class II | Active |
| Pro-V | K073263 | FDA 510(k) | Class II | Active |
| Biscover Lv | K043168 | FDA 510(k) | Class II | Active |
| TheraCem | K161256 | FDA 510(k) | Class II | Active |
| C-Post | K945370 | FDA 510(k) | Class I | Active |
| Diapex | K033585 | FDA 510(k) | Class II | Active |
| Renew Ls-2 | K003361 | FDA 510(k) | Class II | Active |
| Ntl-Flow | K974483 | FDA 510(k) | Class II | Active |
| Pyramid | K982645 | FDA 510(k) | Class II | Active |
| Tesceraflo A2, Model T-21012p; Tesceraflo A2 Opaque, Model T-210120p | K030951 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Recalls (2)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
Bisco Inc. has two recall records, both initiated on 2008-04-28, with a status of terminated. The recalls pertain to BISCEM Self-Adhesive Luting Cement, where stability testing revealed that the product, when used in self-cure mode without light-curing, may exceed the specified setting time and exhibit reduced bond strength. The records do not indicate any additional reasons or variations in the recall scope.
AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Apr 28, 2008 | Z-1696-2008 | — | terminated | During product stability testing, Bisco determined that after 15 months of storage, BISCEM Self-Adhesive Luting Cement used in self-cure mode only without light-curing may take longer than specified to set, resulting in reduced bond strength. Bisco also determined that product component(s) may thicken slightly over time. |
| Apr 28, 2008 | Z-1697-2008 | — | terminated | During product stability testing, Bisco determined that after 15 months of storage, BISCEM Self-Adhesive Luting Cement used in self-cure mode only without light-curing may take longer than specified to set, resulting in reduced bond strength. Bisco also determined that product component(s) may thicken slightly over time. |