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BISCO 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
LinkedIn
—
Facebook
—
Phone
+1(847)534-6000
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
053529939

Catalogue (1223)

Page 6 of 25
DeviceModel / ReferenceRegistriesClassStatus
C&B Base Natural w/F 4gm Syr B-2213QF
FDA UDI
Class IIUnknown
All-Bond Universal B-73050K
FDA UDI
Class IUnknown
Accessory X-80243R
FDA UDI
Class IActive
TheraCal PT H-34111
FDA UDI
Class IIActive
Pro-V C&B A3 50ml Syr. Refill Pkg H-403A3P
FDA UDI
Class IIUnknown
Core-Flo DC Lite A-17803
FDA UDI
Class IIUnknown
CHOICE 2 Ven. Cement D2 4.5gm C-411D2
FDA UDI
Class IIUnknown
TheraCal LC H-3302S
FDA UDI
Class IIActive
TheraCem Ca D-46502PS
FDA UDI
Class IUnknown
Aelite Aesthetic Enamel H-854B4
FDA UDI
Class IIUnknown
Light-Core A-1727P
FDA UDI
Class IIUnknown
Porcelain Etchant E-5720E
FDA UDI
Class IIUnknown
Choice 2 C-3900K-EU
FDA UDI
Class IIUnknown
Opaquer B-2112Q
FDA UDI
Class IIUnknown
Porcelain Bonding Resin B-3110
FDA UDI
Class IIUnknown
Aelite Aesthetic Enamel H-852A3P
FDA UDI
Class IIUnknown
AELITE LS C2 15tips/Fex Tube H-722C2F
FDA UDI
Class IIUnknown
Ace Universal Primer A&B 1Cartridge PKG B-41210P
FDA UDI
Class IUnknown
Choice 2 C-411A1
FDA UDI
Class IIUnknown
Aeliteflo H-674D3F
FDA UDI
Class IIUnknown
Resinomer D/C Base 4g D-43001R
FDA UDI
Class IIUnknown
DT Drill #1 (Pkg of 2) X-80781P
FDA UDI
Class IUnknown
TheraCal PT H-34111P
FDA UDI
Class IIActive
Duo-Link Universal A-19031PS
FDA UDI
Class IIActive
All-Bond SE Part II 6ml in Bag U-3002P
FDA UDI
Class IIUnknown
All-Bond Universal B-72020K
FDA UDI
Class IIUnknown
Bisfil 2B A-1254P
FDA UDI
Class IIUnknown
Aeliteflo LV H-664A35F
FDA UDI
Class IIUnknown
DT LIGHT POST #3 (Pkg.of 10) X-80753P
FDA UDI
Class IUnknown
AELITE-All Purpose Body D3 UD H-814D3
FDA UDI
Class IIUnknown
eCement C-5201
FDA UDI
Class IIUnknown
Opaquer B-2122
FDA UDI
Class IIActive
Try In Paste C2 2g C-412C2
FDA UDI
Class IIUnknown
All-Bond 3 B-3601
FDA UDI
Class IIActive
Aelite Aesthetic Enamel H-852D4
FDA UDI
Class IIUnknown
Choice 2 C-411MO
FDA UDI
Class IIUnknown
Porcelain Primer B-2223P
FDA UDI
Class IIActive
CHOICE 2 Ven. Cement B3 4.5gm C-411B3
FDA UDI
Class IIUnknown
Quantium H-120ICS
FDA UDI
Class IIActive
All-Bond Universal B-7206S
FDA UDI
Class IIActive
eCement Try-In Paste C-531MBP
FDA UDI
Class IUnknown
Aelite Aesthetic Enamel H-854W2
FDA UDI
Class IIActive
Duo-Link Universal A-19620K
FDA UDI
Class IIUnknown
Z-Prime Plus B-6003PS
FDA UDI
Class IIUnknown
Core-Flo DC Lite A-17801SP
FDA UDI
Class IUnknown
Aeliteflo H-671A35F
FDA UDI
Class IActive
Choice 2 C-411MBP
FDA UDI
Class IIUnknown
Transluma ISO#90 Drill 2ea X-81621
FDA UDI
Class IUnknown
Light-Core A-1727P
FDA UDI
Class IIActive
C&B (1 Dual Syr) Pkg - Opaque B-22110P
FDA UDI
Class IIUnknown

Related Companies

Authorised Representatives

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Importers

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Notified Bodies

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Authorities

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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.

DateRecall No.ClassStatusReason
Apr 28, 2008Z-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, 2008Z-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.