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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 33 of 111
DeviceModel / ReferenceRegistriesClassStatus
Tinto Calretinin, RMab Predilute, 7 ml
FDA UDI
Class IActive
Tinto PSAP (RBT-PSAP) BSB-3846-7
FDA UDI
Class IActive
TdT control slides Control Slides, 5
FDA UDI
Class IActive
ZFAND3 Control Slides BSB-9435-CS
FDA UDI
Class IActive
Tinto SOX-2 , RMab Predilute, 7 ml
FDA UDI
Class IActive
CA-125 Control Slides BSB-9046-CS
FDA UDI
Class IActive
CXCR4/CD184/Fusin Control Slides BSB-9127-CS
FDA UDI
Class IActive
Tinto Claudin 18.2 (RBT-CLDN18.2) BSB-3835-3-ASR
FDA UDI
Class IActive
bcl-6 control slides Control Slides, 5
FDA UDI
Class IActive
Tinto S100A9 RMab Predilute, 3 ml
FDA UDI
Class IActive
TSH Control Slides Control Slides, 5
FDA UDI
Class IActive
Tinto CDX2 (RBT-CDX2) BSB-3819-15
FDA UDI
Class IActive
HPV16 Control Slides BSB-9226-CS
FDA UDI
Class IActive
CD8 Control Slides BSB-9112-CS
FDA UDI
Class IActive
Tinto Synaptophysin (RBT-Synaptophysin) BSB-3811-7
FDA UDI
Class IActive
Androgen Receptor Control Slides BSB-9016-CS
FDA UDI
Class IActive
Renal Cell Carcinoma Control Slides Control Slides, 5
FDA UDI
Class IActive
ImmunoRetriever 20X with EDTA 1000 ml
FDA UDI
Class IActive
Cytokeratin 7 & CDX2 RMab Concentrate, 1 ml
FDA UDI
Class IActive
hCG control slides Control Slides, 5
FDA UDI
Class IActive
Tinto Toxoplasma gondii, RPab Predilute, 7 ml
FDA UDI
Class IActive
Mouse/Rabbit PolyDetector Plus Link & HRP Label Ready-to-use, 100 ml each
FDA UDI
Class IActive
3-core ALK Cell Line Microarray Control Slides Control Slides, 5
FDA UDI
Class IActive
Cytokeratin 5 & 14 control slides Control Slides, 5
FDA UDI
Class IActive
Cytokeratin 8 &18 control slides Control Slides, 5
FDA UDI
Class IActive
TintoReagent Rack BSB-7465
FDA UDI
Class IActive
Clusterin/ Apolipoprotein J RMab Concentrate, 1 ml
FDA UDI
Class IActive
Tinto MSH2, MMab Predilute, 7 ml
FDA UDI
Class IActive
MUC-4 control slides Control Slides, 5
FDA UDI
Class IActive
HBV Cell Line Array (2-core: Positive and Negative) Control Slides Control Slides, 5
FDA UDI
Class IActive
Mouse/Rabbit ImmunoDetector Biotin Link Ready-to-use, 100 ml
FDA UDI
Class IActive
CD14 control slides Control Slides, 5
FDA UDI
Class IActive
Tinto CD138 (RBT-CD138) BSB-3817-7
FDA UDI
Class IActive
CD5 RMab Concentrate, 0.5 ml
FDA UDI
Class IActive
PolyDetector HRP Blue Plus BSB-0363-100
FDA UDI
Class IActive
3-core Androgen Receptor Cell Line Microarray Control Slides Control Slides, 5
FDA UDI
Class IActive
Chromogranin A Control Slides Control Slides, 5
FDA UDI
Class IActive
Mouse/Rabbit PolyDetector HRP Label Ready-to-use, 15 ml each
FDA UDI
Class IActive
WT1 control slides Control Slides, 5
FDA UDI
Class IActive
Tinto IgG, RPab Predilute, 7 ml
FDA UDI
Class IActive
FluoroMounter 100 ml
FDA UDI
Class IActive
CD117 c-Kit PolyDetector DAB HRP Brown 70 tests
FDA UDI
Class IActive
Ksp-Cadherin Control Slides BSB-9252-CS
FDA UDI
Class IActive
Ezh2 (rbt-Ezh2) BSB-3823-1
FDA UDI
Class IActive
Herpes Simplex Virus I RPab Concentrate, 1 ml
FDA UDI
Class IActive
TintoHematoxylin Automation 50 ml
FDA UDI
Class IActive
PMS2 Control Slides Control Slides, 5
FDA UDI
Class IActive
Somatostatin RPab Concentrate, 0.1 ml
FDA UDI
Class IActive
Tinto A-1-Antichymotrypsin RPab Predilute, 7 ml
FDA UDI
Class IActive
Cytokeratin HMW AE3 control slides Control Slides, 5
FDA UDI
Class IActive

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