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BIO SB, INC.

United States·US-MF-000036462

Last updated September 17, 2026

What BIO SB, INC. makes

Bio SB, Inc. manufactures in vitro diagnostic (IVD) products for immunohistochemistry, including chromogenic substrates, enzyme-linked detection kits, and antibody-based reagents. Their portfolio includes enzyme immunohistochemistry substrates like DAB and AEC, as well as specific detection antibodies such as cytokeratin and CD cell markers. Control slides and reagents for analytes like Helicobacter pylori, Candida albicans, and BAP1 are also produced, alongside specialized digestion solutions for tissue processing.

The company’s products are classified under FDA’s Class I medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. These devices are intended for laboratory use in diagnostic testing and are regulated under U.S. FDA guidelines. The manufacturer operates within 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 Bio SB, Inc. manufacture?

Bio SB, Inc. specializes in in vitro diagnostic (IVD) products primarily used in immunohistochemistry (IHC) testing. Their portfolio includes chromogenic substrates like DAB (brown) and AEC (red) for enzyme-linked detection, antibody-based reagents for detecting specific analytes (such as cytokeratin and CD cell markers), and control slides for validation purposes. Examples include reagents for Helicobacter pylori, Candida albicans, and specialized tissue digestion solutions like the Mohs ImmunoDigestor. These products are designed for laboratory use in diagnostic workflows.

Where is Bio SB, Inc. based, and how does that affect its regulatory standing?

Bio SB, Inc. is based in the United States. Since it manufactures devices regulated by the FDA, its products must comply with U.S. regulatory requirements. The company’s devices fall under FDA’s Class I classification, which generally involves lower-risk devices requiring less stringent premarket review. However, compliance with FDA guidelines—such as listing in the UDI database—remains essential for market authorization.

Which regulatory registries or databases list Bio SB, Inc.’s devices?

Bio SB, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system is a standardized way for the FDA to track and identify medical devices in the U.S. market. Listing in this database ensures traceability and compliance with FDA requirements for Class I devices, though it does not imply individual device approval—only that the manufacturer has registered their products as required.

How are Bio SB, Inc.’s devices classified by regulatory authorities?

Bio SB, Inc.’s devices are classified under the FDA’s Class I category. This classification is based on risk assessment: Class I devices are generally considered low-risk and pose minimal potential harm to users. As a result, they typically require less regulatory oversight than higher-risk classes (e.g., Class II or III), though they must still meet FDA compliance standards, such as proper labeling, manufacturing controls, and UDI registration. Classification does not guarantee market authorization—only that the device falls under a specific regulatory pathway.

What is the primary purpose of Bio SB, Inc.’s in vitro diagnostic (IVD) products?

Bio SB, Inc.’s IVD products are designed for laboratory use in immunohistochemistry (IHC) and related diagnostic testing. These include chromogenic substrates (e.g., DAB for brown staining), antibody reagents for detecting specific proteins (like cytokeratin or CD markers), and control slides to validate test accuracy. For example, their Helicobacter pylori control slides or BAP1 antibodies help pathologists confirm the presence of specific biomarkers in tissue samples. The products support accurate diagnostic workflows in clinical or research settings.

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

Information

Country
United States
Address
5385 , Hollister Avenue, Santa Barbara, CA, United States
Website
biosb.com
LinkedIn
—
Facebook
—
Phone
+1(800)561-1145
PRRC Contact
Jessica Dunston
EUDAMED SRN
US-MF-000036462
FDA FEI Number
3008773547
DUNS Number
102855447

Catalogue (5547)

Page 89 of 111
DeviceModel / ReferenceRegistriesClassStatus
Tinto Cytokeratin 4, EP4, RMab BSB 6592
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast Podoplanin, D2-40, MMab BSB-3699-3
EUDAMEDFDA UDI
IVD GeneralActive
Nanog, EP225, RMab BSB 3585
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Factor VIII-Related Antigen, Polyclonal, RPab BSB 5500
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Epstein Barr Virus LMP-1, CS1-4, MMab BSB 5484
EUDAMEDFDA UDI
IVD GeneralActive
Tinto GFAP, RM246, RMab BSB-3766-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Mycobacterium tuberculosis, Polyclonal, RPab BSB 2994
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CEACAM7, BSB-168, MMab BSB-3791-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD2, AB75, MMab BSB 6206
EUDAMEDFDA UDI
IVD GeneralActive
Topoisomerase IIa, RBT-Topo2a, RMab BSB 6342
EUDAMEDFDA UDI
IVD GeneralActive
Tinto HER2 neu, EP3, RMab BSB 2510
EUDAMEDFDA UDI
IVD GeneralActive
Progesterone Receptor, RBT-22, RMab BSB 5886
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 4, EP4, RMab BSB 6591
EUDAMEDFDA UDI
IVD GeneralActive
ATM, EP327, RMab BSB-3710-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto BOB.1, RBT BOB.1, RMab BSB-3700-3
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast EMA, E29, MMab BSB-3692-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto C3c|FITC, Polyclonal, RPab BSB-3002-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto pTau Phospho|Thr 181, BSB-176, MMab BSB-3807-15
EUDAMEDFDA UDI
IVD GeneralActive
Caspase-3, RM250, RMab BSB-3715-01
EUDAMEDFDA UDI
IVD GeneralActive
bcl-6, BSB-26, MMab BSB 3438
EUDAMEDFDA UDI
IVD GeneralActive
Caldesmon, BSB-19, MMab BSB 6103
EUDAMEDFDA UDI
IVD GeneralActive
CD23, EP75, RMab BSB 6476
EUDAMEDFDA UDI
IVD GeneralActive
TIA-1, TIA-1, MMab BSB 6357
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Lambda|FITC, Polyclonal, GPab BSB-3010-15
EUDAMEDFDA UDI
IVD GeneralActive
Cyclin D1, RBT-14, RMab BSB 5368
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 7, OV-TL 12|30, MMab BSB 5409
EUDAMEDFDA UDI
IVD GeneralActive
CD25, RBT-CD25, RMab BSB 2458
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 20, EP23, RMab BSB 6704
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TIA-1, RBT-TIA1, RMab BSB-3782-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD138, EP201, RMab BSB 6529
EUDAMEDFDA UDI
IVD GeneralActive
Progesterone Receptor, BSB-2, MMab BSB 2129
EUDAMEDFDA UDI
IVD GeneralActive
Tinto T-Bet|TBX-2, EP263, RMab BSB 2601
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD137|TNFRSF9, BSB-159, MMab BSB-3717-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto FOXP3, Polyclonal, RPab BSB 6760
EUDAMEDFDA UDI
IVD GeneralActive
DOG-1, RBT-DOG1, RMab BSB 6273
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD63, NKI|C3, MMab BSB 6298
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MUC1, BSB-44, MMab BSB 6149
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MDR-1, JSB-1, MMab BSB 6900
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 7, OV-TL 12|30, MMab BSB 5412
EUDAMEDFDA UDI
IVD GeneralActive
Uroplakin III, Polyclonal, RPab BSB 2291
EUDAMEDFDA UDI
IVD GeneralActive
Tinto COX-2, RBT-COX2, RMab BSB 5360
EUDAMEDFDA UDI
IVD GeneralActive
Calponin, BSB-20, MMab BSB 5123
EUDAMEDFDA UDI
IVD GeneralActive
STAR, EP226, RMab BSB 3635
EUDAMEDFDA UDI
IVD GeneralActive
CD142|TF|Coagulation Factor III, BSB-143, MMab BSB-3718-01
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Survivin, EP119, RMab BSB 2224
EUDAMEDFDA UDI
IVD GeneralActive
SATB2, EP281, RMab BSB 3201
EUDAMEDFDA UDI
IVD GeneralActive
Tinto INI-1, 25, MMab BSB 6829
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cyclin E1, EP126, RMab BSB 6556
EUDAMEDFDA UDI
IVD GeneralActive
Tinto HIF-1alpha, EP118, RMab BSB 2519
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cyclin E1, EP126, RMab BSB 6557
EUDAMEDFDA UDI
IVD GeneralActive

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