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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 29 of 111
DeviceModel / ReferenceRegistriesClassStatus
Muc4 (rbt-Muc4) BSB-3841-05
FDA UDI
Class IActive
Glut1 (rbt-Glut1) BSB-3824-01
FDA UDI
Class IActive
PLAP control slides Control Slides, 5
FDA UDI
Class IActive
Smoothelin MMab Concentrate, 0.5 ml
FDA UDI
Class IActive
PolyDetector HRP Blue Plus BSB-0363-500
FDA UDI
Class IActive
Tinto Hepatitis B Virus Surface Antigen, MMab Predilute, 15 ml
FDA UDI
Class IActive
Myosin, Smooth Muscle Heavy Chain control slides Control Slides, 5
FDA UDI
Class IActive
Tinto ROS-1 (EP282) BSB 3623 (ASR)
FDA UDI
Class IActive
Tinto Follicular Dendritic Cell MMab Predilute, 7 ml
FDA UDI
Class IActive
Myeloperoxidase Control Slides BSB-9296-CS
FDA UDI
Class IActive
Alpha Synuclein Control Slides BSB-9011-CS
FDA UDI
Class IActive
Tinto Mycobacterium tuberculosis (Polyclonal) BSB 2994 (ASR)
FDA UDI
Class IActive
Factor VIII-Related Antigen Control Slides Control Slides, 5
FDA UDI
Class IActive
Tinto Treponema pallidum (Polyclonal) BSB 3232 (ASR)
FDA UDI
Class IActive
Tinto GLUT1 (RBT-GLUT1) BSB-3824-15
FDA UDI
Class IActive
HE4 control slides Control Slides, 5
FDA UDI
Class IActive
Tinto Myoglobin, RPab Predilute, 15 ml
FDA UDI
Class IActive
Caldesmon Control Slides Control Slides, 5
FDA UDI
Class IActive
Plastic Staining Dish BSB 7009
FDA UDI
Class IActive
Bap1 (rbt-Bap1) BSB-3839-05
FDA UDI
Class IActive
Mart-1/Melan-A Control Slides BSB-9266-CS
FDA UDI
Class IActive
Thrombomodulin/ CD141 RMab Concentrate, 1 ml
FDA UDI
Class IActive
HLA-DRB1 beta chain RMab Concentrate, 0.1 ml
FDA UDI
Class IUnknown
Mouse/Rabbit ImmunoDetector Biotin Link & AP Label Ready-to-use, 200 ml each
FDA UDI
Class IActive
Mycobacterium tuberculosis (Polyclonal) BSB 2996 (ASR)
FDA UDI
Class IActive
MUC5AC Control Slides BSB-9290-CS
FDA UDI
Class IActive
Cd138 (rbt-Cd138) BSB-3817-05
FDA UDI
Class IActive
SMAD4/DPC4 control slides Control Slides, 5
FDA UDI
Class IActive
Tinto HER2 neu (EP3) BSB 2510 (ASR)
FDA UDI
Class IActive
Caveolin-1 Control Slides BSB-9057-CS
FDA UDI
Class IActive
Cytokeratin 18 Control Slides BSB-9138-CS
FDA UDI
Class IActive
pan-TRK (RBT-TRK) BSB-2376-1-ASR
FDA UDI
Class IActive
Olig2 (rbt-Olig2) BSB-3831-1
FDA UDI
Class IActive
MMP-9 control slides Control Slides, 5
FDA UDI
Class IActive
Estrogen Receptor (RM292) BSB-3765-01-ASR
FDA UDI
Class IActive
CD16 control slides Control Slides, 5
FDA UDI
Class IActive
Tinto FOXA1 / HNF-3A Predilute, 7ml
FDA UDI
Class IActive
Tinto MSH2 MMab Predilute, 15 ml
FDA UDI
Class IActive
Tinto HPV (BSB-66) BSB 5654 (ASR)
FDA UDI
Class IActive
Cytokeratin 17 RMab Concentrate, 0.5 ml
FDA UDI
Class IActive
PolyDetector Liquid DAB HRP Brown kit 2000 tests
FDA UDI
Class IActive
Tinto Cytokeratin 10, RMab Predilute, 3 ml
FDA UDI
Class IActive
FOXP3 RMab Control Slides Control Slides, 5
FDA UDI
Class IActive
Tinto Helicobacter pylori (Polyclonal) BSB 5604 (ASR)
FDA UDI
Class IActive
Cyclin D1 RMab Concentrate, 1 ml
FDA UDI
Class IActive
Tinto Langerin / CD207 RMab Predilute, 7 ml
FDA UDI
Class IActive
CDK2 RMab Control Slides Control Slides, 5
FDA UDI
Class IActive
Calcitonin (RBT-Calcitonin) BSB-3814-05
FDA UDI
Class IActive
PDGFR-B RMab Control Slides Control Slides, 5
FDA UDI
Class IActive
Topoisomerase IIa Control Slides Control Slides, 5
FDA UDI
Class IActive

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