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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 24 of 111
DeviceModel / ReferenceRegistriesClassStatus
Tinto Cytokeratin 15, RMab Predilute, 3 ml
FDA UDI
Class IActive
Bcl-x control slides Control Slides, 5
FDA UDI
Class IActive
S100A6 RMab Concentrate, 1 ml
FDA UDI
Class IActive
Tinto OLIG2 (RBT-OLIG2) BSB-3831-15
FDA UDI
Class IActive
ICOS/CD278 Control Slides BSB-9229-CS
FDA UDI
Class IActive
Helicobacter Pylori Control Slides BSB-9205-CS
FDA UDI
Class IActive
Tinto Helicobacter Pylori (BSB-37) BSB 2678 (ASR)
FDA UDI
Class IActive
Tinto GCDFP-15, RMab Predilute, 7 ml
FDA UDI
Class IActive
HLA-DRB1 beta chain RMab Concentrate, 1 ml
FDA UDI
Class IActive
Smoothelin control slides Control Slides, 5
FDA UDI
Class IActive
Melanoma control slides Control Slides, 5
FDA UDI
Class IActive
Braf V600e (rm8) BSB 2827 (ASR)
FDA UDI
Class IActive
Nuclear Fast Red Counterstainer 50 ml
FDA UDI
Class IActive
Villin control slides Control Slides, 5
FDA UDI
Class IActive
PSA RMab Concentrate, 0.5 ml
FDA UDI
Class IActive
ImmunoRetriever 20X with Citrate 200 ml
FDA UDI
Class IActive
Fascin Control Slides BSB-9177-CS
FDA UDI
Class IActive
Tinto Herpes Simplex Virus I Predilute, 7 ml
FDA UDI
Class IActive
Cytokeratin 35BH11 control slides Control Slides, 5
FDA UDI
Class IActive
IgM control slides Control Slides, 5
FDA UDI
Class IActive
Tinto S100A8/MRP8 (RBT-MRP8) BSB-3847-3
FDA UDI
Class IActive
HSP70 Control Slides BSB-9228-CS
FDA UDI
Class IActive
TintoPolyDetector Plus Brown Detection Kit (300 Test) BSB-7462
FDA UDI
Class IActive
Tinto HLA-DRB1 beta chain RMab Predilute, 7 ml
FDA UDI
Class IUnknown
NKX3.1 control slides Control Slides, 5
FDA UDI
Class IActive
Prealbumin/Transthyretin Control Slides BSB-9352-CS
FDA UDI
Class IActive
Tinto Herpes Simplex Virus II (Polyclonal) BSB 2335 (ASR)
FDA UDI
Class IActive
Tinto E2F4, RMab Predilute,15 ml
FDA UDI
Class IActive
PSP94/MSMB, RMab Concentrate, 1 ml
FDA UDI
Class IActive
MyoD1 (RBT-MYOD1) BSB-3829-01
FDA UDI
Class IActive
HER-2 neu (RBT-HER2) BSB 2038 (ASR)
FDA UDI
Class IActive
Tinto Cadherin-6, RMab Predilute, 15 ml
FDA UDI
Class IActive
Tinto CD4 (BSB-179) BSB-3818-3
FDA UDI
Class IActive
FOXO1 RMab Concentrate, 1 ml
FDA UDI
Class IActive
Tinto Histone H3 Phospho (RBT-pHH3) BSB-3844-3
FDA UDI
Class IActive
Cyclin D1 RMab Concentrate, 0.1 ml
FDA UDI
Class IActive
Tinto S100A9 RMab Predilute, 15 ml
FDA UDI
Class IActive
TdT Control Slides BSB-9403-CS
FDA UDI
Class IActive
p21 Control Slides BSB-9322-CS
FDA UDI
Class IActive
Beta-Catenin RMab Concentrate, 0.1 ml
FDA UDI
Class IActive
CDK4 Control Slides BSB-9115-CS
FDA UDI
Class IActive
Cytokeratin 15 control slides Control Slides, 5
FDA UDI
Class IActive
Ros-1 (ep282) BSB 3626 (ASR)
FDA UDI
Class IActive
Tinto Progesterone Receptor (EP2) BSB 2573 (ASR)
FDA UDI
Class IActive
Estrogen Receptor (BSB-1) BSB 2745 (ASR)
FDA UDI
Class IActive
PolyDetector Liquid AEC HRP Red Ready-To-use, 1000 ml
FDA UDI
Class IActive
Tinto Estrogen Receptor (EP1) BSB 2491 (ASR)
FDA UDI
Class IActive
Mesothelin RMab Concentrate, 0.5 ml
FDA UDI
Class IActive
PAX-8 Control Slides BSB-9337-CS
FDA UDI
Class IActive
MNDA Control Slides BSB-9283-CS
FDA UDI
Class IActive

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