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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 95 of 111
DeviceModel / ReferenceRegistriesClassStatus
TMPRSS2, BSB-136, MMab BSB-3703-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Neurofilament, 2F11, MMab BSB 5815
EUDAMEDFDA UDI
IVD GeneralActive
Tinto FOXP1, EP137, RMab BSB 6751
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Tri-Methyl-Histone H3(Lys27)|H3K27Me3, RBT-H3K27Me3, RMab BSB-3806-7
EUDAMEDFDA UDI
IVD GeneralActive
Brachyury, RBT-TBXT, RMab BSB 3493
EUDAMEDFDA UDI
IVD GeneralActive
Surfactant protein D|SP-D, BSB-162, MMab BSB-3747-01
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Ksp-Cadherin, 4H6|F9, MMab BSB 6282
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD25, 4C9, MMab BSB 6319
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PDX1, EP139, RMab BSB 3157
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD61, EP65, RMab BSB 3511
EUDAMEDFDA UDI
IVD GeneralActive
Kappa Light Chains, BSB-58, MMab BSB 5706
EUDAMEDFDA UDI
IVD GeneralActive
ACE2, BSB-135, MMab BSB-3702-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CEA, BSB-13, MMab BSB 5337
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p16, 16P04, JC2, MMab BSB 5828
EUDAMEDFDA UDI
IVD GeneralActive
Tinto bcl-6, BSB-26, MMab BSB 3435
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Calponin, BSB-20, MMab BSB 5121
EUDAMEDFDA UDI
IVD GeneralActive
CD3 Epsilon, RBT-CD3e, RMab BSB 5145
EUDAMEDFDA UDI
IVD GeneralActive
IgA, BSB-39, MMab BSB 5662
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin OSCAR, OSCAR, MMab BSB 6177
EUDAMEDFDA UDI
IVD GeneralActive
Claudin-5, EP224, RMab BSB 2401
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Myoglobin, BSB-104, MMab BSB 3384
EUDAMEDFDA UDI
IVD GeneralActive
IgG4, EP138, RMab BSB 6817
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 8 and 18, B22.1 and B23.1, MMab BSB 5418
EUDAMEDFDA UDI
IVD GeneralActive
Hepatocyte Specific Antigen\Hep-Par1, OCH1E5, MMab BSB 5628
EUDAMEDFDA UDI
IVD GeneralActive
Renal Cell Carcinoma, PN-15, MMab BSB 5914
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Herpes Simplex Virus I, 10A3, MMab BSB 2684
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD34, EP88, RMab BSB 6485
EUDAMEDFDA UDI
IVD GeneralActive
CD16, EP364, RMab BSB 3324
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Surfactant protein D|SP-D, BSB-162, MMab BSB-3747-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD68, KP-1, MMab BSB 2714
EUDAMEDFDA UDI
IVD GeneralActive
GAB1|GRB2-associated-binding protein 1, BSB-155, MMab BSB-3727-1
EUDAMEDFDA UDI
IVD GeneralActive
Melanoma Cocktail: HMB-45, MART-1 and Tyrosinase, HMB-45, A103 and BSB-6, MMab BSB 6882
EUDAMEDFDA UDI
IVD GeneralActive
IgA|FITC, Polyclonal, GPab BSB-3005-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 8, EP17, RMab BSB 6660
EUDAMEDFDA UDI
IVD GeneralActive
Tau, BSB-115, MMab BSB 3430
EUDAMEDFDA UDI
IVD GeneralActive
Progesterone Receptor, EP2, RMab BSB 2578
EUDAMEDFDA UDI
IVD GeneralActive
Tinto BCOR, BSB-128, MMab BSB-2370-3
EUDAMEDFDA UDI
IVD GeneralActive
PD-L1|CD274, 28-8, RMab BSB-2371-01
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 18, EP30, RMab BSB 6698
EUDAMEDFDA UDI
IVD GeneralActive
IgG4, BSB-96, MMab BSB 6812
EUDAMEDFDA UDI
IVD GeneralActive
CD147, BSB-137, MMab BSB-3704-01
EUDAMEDFDA UDI
IVD GeneralActive
Tinto C4c|FITC, Polyclonal, RPab BSB-3003-7
EUDAMEDFDA UDI
IVD GeneralActive
IgA|FITC, Polyclonal, GPab BSB-3005-1
EUDAMEDFDA UDI
IVD GeneralActive
SOX-2, RM427, RMab BSB-3770-01
EUDAMEDFDA UDI
IVD GeneralActive
PTEN, RM265, RMab BSB-3769-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MSH2, RBT-MSH2, RMab BSB 6926
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ARID1A, EP303, RMab BSB-3749-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin OSCAR, OSCAR, MMab BSB 6178
EUDAMEDFDA UDI
IVD GeneralActive
Melanosome HMB45, HMB-45, MMab BSB 5762
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MUC2, EP187, RMab BSB 6948
EUDAMEDFDA UDI
IVD GeneralActive

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