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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 48 of 111
DeviceModel / ReferenceRegistriesClassStatus
CD123 control slides Control Slides, 5
FDA UDI
Class IActive
Thyroglobulin Control Slides Control Slides, 5
FDA UDI
Class IActive
Retinoblastoma/ Rb control sldies Control Slides, 5
FDA UDI
Class IActive
Tinto NKX6.1 (RBT-NKX6.1) BSB-3836-15
FDA UDI
Class IActive
CD71 control slides Control Slides, 5
FDA UDI
Class IActive
TdT control slides Control Slides, 5
FDA UDI
Class IActive
Tinto Smoothelin RMab Predilute, 7 ml
FDA UDI
Class IActive
Tinto Spectrin, RMab Prediluted, 15 ml
FDA UDI
Class IActive
Tinto LEF1 (RBT-LEF1) BSB-3826-3
FDA UDI
Class IActive
PolyDetector HRP Mulberry BSB-0362-100
FDA UDI
Class IActive
Tinto PMS2 (RBT-PMS2) BSB-3832-3
FDA UDI
Class IActive
Herpes Simplex Virus I Control Slides Control Slides, 5
FDA UDI
Class IActive
PDX1 control slides Control Slides, 5
FDA UDI
Class IActive
Toxoplasma gondii control slides Control Slides, 5
FDA UDI
Class IActive
Tinto Thrombomodulin RMab Predilute, 3 ml
FDA UDI
Class IActive
LRG1 Control Slides BSB-9440-CS
FDA UDI
Class IActive
c-Myc (RBT-CMYC) BSB-3813-1
FDA UDI
Class IActive
PolyDetector Alk Brown Ready-To-Use 50 ml
FDA UDI
Class IActive
Myelin Basic Protein Control Slides BSB-9295-CS
FDA UDI
Class IActive
PolyDetector HRP Fuchsia BSB-0364-1000
FDA UDI
Class IActive
CD75 control slides Control Slides, 5
FDA UDI
Class IActive
Herpes Simplex Virus I (Polyclonal) BSB 2431 (ASR)
FDA UDI
Class IActive
9-core HER-2 Cell Line Microarray (0, +, 1+, 2+, 3+ in duplicates) Control Slide Control Slides, 5
FDA UDI
Class IActive
GATA3 Control Slides BSB-9192-CS
FDA UDI
Class IActive
Tinto S100A8/MRP8, RMab Predilute, 7 ml
FDA UDI
Class IActive
Oct4/Pou5f1 (rbt-Oct4) BSB-3830-05
FDA UDI
Class IActive
Tinto GLUT1 (RBT-GLUT1) BSB-3824-3
FDA UDI
Class IActive
FluoroMounter with DAPI 100 ml
FDA UDI
Class IActive
Mouse/Rabbit PolyDetector Plus Link & HRP Label Ready-to-use, 50 ml each
FDA UDI
Class IActive
CD13 control slides Control Slides, 5
FDA UDI
Class IActive
Galectin-3 Control Slides BSB-9190-CS
FDA UDI
Class IActive
Tinto CTLA-4/CD152 (RBT-CTLA-4) BSB 3483 (ASR)
FDA UDI
Class IActive
MCM5 RMab Concentrate, 1 ml
FDA UDI
Class IActive
CD4 Control Slides BSB-9090-CS
FDA UDI
Class IActive
Rabbit Negative Control 3 ml
FDA UDI
Class IActive
Calponin Control Slides BSB-9053-CS
FDA UDI
Class IActive
Tinto MCM5, RMab Predilute, 15 ml
FDA UDI
Class IActive
Neun control slides Control Slides, 5
FDA UDI
Class IActive
TIM-3/HAVCR2/CD366 Control Slides BSB-9411-CS
FDA UDI
Class IActive
SDHB, Control Slides Control Slides, 5
FDA UDI
Class IActive
Tinto Herpes Simplex Virus I (Polyclonal) BSB 2427 (ASR)
FDA UDI
Class IActive
Myosin Smooth Muscle Control Slides BSB-9300-CS
FDA UDI
Class IActive
Tinto CD15, RMab Predilute, 7 ml
FDA UDI
Class IActive
Tinto Cytokeratin 5 & 6 & ERG, RMab Predilute, 3 ml
FDA UDI
Class IActive
Varicella Zoster Virus (SG1, SG1-1, SG2-2E6, SG3, SG4, NCP-1 & IE-62) BSB-3810-05-ASR
FDA UDI
Class IActive
Prolactin (RBT-PRL) BSB-3845-1
FDA UDI
Class IActive
MDR-1 RMab Concentrate, 1 ml
FDA UDI
Class IActive
Cytokeratin 7 Control Slides BSB-9149-CS
FDA UDI
Class IActive
Osteonectin/SPARC control slides Control Slides, 5
FDA UDI
Class IActive
Tinto Calcitonin RPab Predilute, 15 ml
FDA UDI
Class IActive

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