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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 82 of 111
DeviceModel / ReferenceRegistriesClassStatus
Thyroglobulin, 2H11 and 6E1, MMab BSB 2766
EUDAMEDFDA UDI
IVD GeneralActive
Tinto B7H3|CD276, RBT-B7H3, RMab BSB 2811
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast EMA, E29, MMab BSB-3692-3
EUDAMEDFDA UDI
IVD GeneralActive
CD23, 1B12, MMab BSB 5208
EUDAMEDFDA UDI
IVD GeneralActive
CEA, Polyclonal, RPab BSB 6539
EUDAMEDFDA UDI
IVD GeneralActive
CD71, 10F11, MMab BSB 6524
EUDAMEDFDA UDI
IVD GeneralActive
GATA3, L50-823, MMab BSB 2673
EUDAMEDFDA UDI
IVD GeneralActive
BCOR, BSB-128, MMab BSB-2370-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TdT, RBT-TdT, RMab BSB 2266
EUDAMEDFDA UDI
IVD GeneralActive
Tinto EpCAM|Epithelial Specific Antigen, MOC-31, MMab BSB 6723
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Amyloid A, EP335, RMab BSB 2805
EUDAMEDFDA UDI
IVD GeneralActive
HER2 neu, EP3, RMab BSB 2513
EUDAMEDFDA UDI
IVD GeneralActive
Napsin A, RBT-NAPSA, RMab BSB-3789-01
EUDAMEDFDA UDI
IVD GeneralActive
PLA2R1, BSB-129, MMab BSB-2372-1
EUDAMEDFDA UDI
IVD GeneralActive
SALL4, 6E3, MMab BSB 3187
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD3 Epsilon, RBT-CD3e, RMab BSB 5143
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Napsin A, EP205, RMab BSB 6988
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Langerin, 12D6, MMab BSB 6842
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p40, ZR8, RMab BSB 2070
EUDAMEDFDA UDI
IVD GeneralActive
Synaptophysin, Polyclonal, RPab BSB 5949
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PGP 9.5, BSB-46, MMab BSB 2112
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Perforin, 5B10, MMab BSB 2105
EUDAMEDFDA UDI
IVD GeneralActive
Cyclin E1, EP126, RMab BSB 6558
EUDAMEDFDA UDI
IVD GeneralActive
WT1, 6F-H2, MMab BSB 6032
EUDAMEDFDA UDI
IVD GeneralActive
Mesothelial Cell, HBME-1, MMab BSB 3458
EUDAMEDFDA UDI
IVD GeneralActive
CEA, BSB-13, MMab BSB 5342
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Islet 1|ISL1, EP283, RMab BSB 2973
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TLE1, 1F5, MMab BSB 2316
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MSH6, 44, MMab BSB 6144
EUDAMEDFDA UDI
IVD GeneralActive
Annexin VII, EP367, RMab BSB-3709-1
EUDAMEDFDA UDI
IVD GeneralActive
STAR, EP226, RMab BSB 3634
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cyclin D1, RBT-14, RMab BSB 5367
EUDAMEDFDA UDI
IVD GeneralActive
Tinto A-1-Antitrypsin, Polyclonal, RPab BSB 5010
EUDAMEDFDA UDI
IVD GeneralActive
Prolactin, EP193, RMab BSB 2137
EUDAMEDFDA UDI
IVD GeneralActive
NKX2.2, EP336, RMab BSB 3109
EUDAMEDFDA UDI
IVD GeneralActive
BCA-225, Cu-18, MMab BSB 5069
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 8, EP17, RMab BSB 6664
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TdT, EP266, RMab BSB 2609
EUDAMEDFDA UDI
IVD GeneralActive
CD3 Epsilon, RBT-CD3e, RMab BSB 5146
EUDAMEDFDA UDI
IVD GeneralActive
HMGA2, EP398, RMab BSB-3729-01
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Mart-1|Melan-A, A103, MMab BSB 6870
EUDAMEDFDA UDI
IVD GeneralActive
Bax, E63, RMab BSB 6083
EUDAMEDFDA UDI
IVD GeneralActive
NKX3.1, RM430, RMab BSB-3785-1
EUDAMEDFDA UDI
IVD GeneralActive
MCM3, EP202, RMab BSB 6888
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD5, RM314, RMab BSB-3759-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SALL4, EP299, RMab BSB 3192
EUDAMEDFDA UDI
IVD GeneralActive
Tinto FOXP1, EP137, RMab BSB 6752
EUDAMEDFDA UDI
IVD GeneralActive
DDR1, BSB-173, MMab BSB-3801-01
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD13, 38C12, MMab BSB 6326
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Glypican-3, 1G12, MMab BSB 6242
EUDAMEDFDA UDI
IVD GeneralActive

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