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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 74 of 111
DeviceModel / ReferenceRegistriesClassStatus
Tinto Factor VIII-Related Antigen, Polyclonal, RPab BSB 5499
EUDAMEDFDA UDI
IVD GeneralActive
HHV-8, RBT-HHV8, RMab BSB-3778-01
EUDAMED
IVD GeneralActive
Tinto TLE1, BSB-142, MMab BSB-3784-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CDK4, EP180, RMab BSB 2462
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MCM3, EP202, RMab BSB 6886
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Granzyme B, EP230, RMab BSB 2407
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SMAD4|DPC4, RBT-SMAD4, RMab BSB 3401
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Thyroglobulin, BSB-49, MMab BSB 5974
EUDAMEDFDA UDI
IVD GeneralActive
Arginase-1, EP261, RMab BSB 2452
EUDAMEDFDA UDI
IVD GeneralActive
TAG-72, BSB-21, MMab BSB 5957
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Albumin, polyclonal, RPab BSB 3012
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD61, EP65, RMab BSB 3513
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Inhibin alpha, EP378, RMab BSB 3358
EUDAMEDFDA UDI
IVD GeneralActive
Prolactin, EP193, RMab BSB 2136
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Vimentin, EP21, RMab BSB 2307
EUDAMEDFDA UDI
IVD GeneralActive
Granzyme B, EP230, RMab BSB 2408
EUDAMEDFDA UDI
IVD GeneralActive
CD138, EP201, RMab BSB 6530
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Synaptophysin, Polyclonal, RPab BSB 5945
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast Androgen Receptor, BSB-4, MMab BSB-3690-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Retinoblastoma| Rb, 1F8, MMab BSB 6127
EUDAMEDFDA UDI
IVD GeneralActive
MCM3, EP202, RMab BSB 6889
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PHOX2B, EP312, RMab BSB 3610
EUDAMEDFDA UDI
IVD GeneralActive
Factor VIII-Related Antigen, Polyclonal, RPab BSB 5502
EUDAMEDFDA UDI
IVD GeneralActive
Tinto LAG-3|CD223, EP294, RMab BSB 3365
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CA15-3, DF3, MMab BSB 5099
EUDAMEDFDA UDI
IVD GeneralActive
CTLA-4|CD152, BSB-88, MMab BSB 2883
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Factor XIIIa, EP292, RMab BSB 5507
EUDAMEDFDA UDI
IVD GeneralActive
NUT|NUTM1, RBT-NUTM1, RMab BSB-3793-1
EUDAMEDFDA UDI
IVD GeneralActive
pan-TRK, RBT-TRK, RMab BSB-2376-01
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD43, MT1, MMab BSB 5239
EUDAMEDFDA UDI
IVD GeneralActive
Tinto OCT-2, EP115, RMab BSB 2021
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PAX-2, EP235, RMab BSB 2566
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 7, OV-TL 12|30, MMab BSB 5411
EUDAMEDFDA UDI
IVD GeneralActive
Beta-Catenin, RM276, RMab BSB-3756-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD11c, EP157, RMab BSB 6444
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Tau, BSB-115, MMab BSB 3429
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Beta-Catenin, RM276, RMab BSB-3756-7
EUDAMEDFDA UDI
IVD GeneralActive
CD34, QBEnd|10, MMab BSB 5228
EUDAMEDFDA UDI
IVD GeneralActive
MAGEC2, EP405, RMab BSB-3795-1
EUDAMEDFDA UDI
IVD GeneralActive
CD103|ITGAE, EP206, RMab BSB 2863
EUDAMEDFDA UDI
IVD GeneralActive
SOX-2, RM427, RMab BSB-3770-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Albumin|FITC, polyclonal, RPab BSB-3000-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Helicobacter Pylori, EP279, RMab BSB 3279
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Desmoglein-3, EP306, RMab BSB 2896
EUDAMEDFDA UDI
IVD GeneralActive
Cathepsin K, BSB-172, MMab BSB-3800-01
EUDAMEDFDA UDI
IVD GeneralActive
CA15-3, DF3, MMab BSB 5103
EUDAMEDFDA UDI
IVD GeneralActive
CTLA-4|CD152, RBT-CTLA-4, RMab BSB 3488
EUDAMEDFDA UDI
IVD GeneralActive
bcl-10, BSB-22, MMab BSB 2703
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TORC3|CRTC3, BSB-175, MMab BSB-3805-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Hepatocyte Specific Antigen\Hep-Par1, OCH1E5, MMab BSB 5625
EUDAMEDFDA UDI
IVD GeneralActive

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