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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 12 of 111
DeviceModel / ReferenceRegistriesClassStatus
Epstein Barr Virus LMP-1 Control Slides BSB-9170-CS
FDA UDI
Class IActive
Gastrin Control Slides BSB-9191-CS
FDA UDI
Class IActive
Tinto Hepatitis B Virus Core Antigen (Polyclonal) BSB 5612 (ASR)
FDA UDI
Class IActive
Varicella Zoster Virus (SG1, SG1-1, SG2-2E6, SG3, SG4, NCP-1 & IE-62) BSB-3810-1-ASR
FDA UDI
Class IActive
Tinto Estrogen Receptor (BSB-1) BSB 2740 (ASR)
FDA UDI
Class IActive
NGFR Control Slides BSB-9307-CS
FDA UDI
Class IActive
IgA control slides Control Slides, 5
FDA UDI
Class IActive
Tinto COX-2, RMab Predilute, 15 ml
FDA UDI
Class IActive
Tinto MDM2 (RBT-MDM2) BSB-3827-15
FDA UDI
Class IActive
Mouse/Rabbit AmpliDetector Plus FITC BSB-0359-100
FDA UDI
Class IActive
BAP1 control slides Control Slides, 5
FDA UDI
Class IActive
Cytokeratin 5 & 6 (RM341) BSB-3822-01
FDA UDI
Class IActive
BG8 LewisY Control Slides BSB-9034-CS
FDA UDI
Class IActive
Calretinin Control Slides BSB-9054-CS
FDA UDI
Class IActive
Helicobacter pylori (Polyclonal) BSB 5606 (ASR)
FDA UDI
Class IActive
PolyDetector Alk Scarlet 1000 ml
FDA UDI
Class IActive
Aspergillus (RBT-A.fumi) BSB-3804-1-ASR
FDA UDI
Class IActive
Tinto Hepatitis B Virus Core Antigen, RPab Predilute, 3 ml
FDA UDI
Class IActive
Estrogen Receptor (RBT-11) BSB 5495 (ASR)
FDA UDI
Class IActive
Pink Hematoxylin Counterstainer BSB-0360-100
FDA UDI
Class IActive
7-core PD-L1 Cell Line Microarray Control Slides Control Slides, 5
FDA UDI
Class IActive
Desmoglein-3 Control Slides BSB-9162-CS
FDA UDI
Class IActive
PRAME Control Slides Control Slides, 5
FDA UDI
Class IActive
Immuno/DNA Washer 10X 200 ml
FDA UDI
Class IActive
Estrogen Receptor control slides Control Slides, 5
FDA UDI
Class IActive
AMACRacemase/P504S Control Slides BSB-9013-CS
FDA UDI
Class IActive
Tinto Cytokeratin 7, RMab Predilute, 15 ml
FDA UDI
Class IActive
Adenovirus MMab Concentrate, 0.5 ml
FDA UDI
Class IActive
Tinto c-Myc (RBT-CMYC) BSB-3813-3
FDA UDI
Class IActive
Tinto CTLA-4/CD152 (BSB-88) BSB 2881 (ASR)
FDA UDI
Class IActive
Tinto Herpes Simplex Virus II (BSB-116) BSB 3462 (ASR)
FDA UDI
Class IActive
Herpes Simplex Virus II (BSB-116) BSB 3465 (ASR)
FDA UDI
Class IActive
Mouse/Rabbit PolyDetector Plus Link & HRP Label Ready-to-use, 1000 ml each
FDA UDI
Class IActive
Tinto EZH2 (RBT-EZH2) BSB-3823-3
FDA UDI
Class IActive
Progesterone Receptor (EP2) BSB 2578 (ASR)
FDA UDI
Class IActive
HPV MultiDetector HRP/AP Detection System Kit Ready-to-use, 70 tests each
FDA UDI
Class IActive
Tinto Cytokeratin 8 &18, RMab Predilute, 7 ml
FDA UDI
Class IActive
Tyrosinase Control Slides BSB-9423-CS
FDA UDI
Class IActive
Annexin A1 Control Slides BSB-9017-CS
FDA UDI
Class IActive
Cytokeratin 4 control slides Control Slides, 5
FDA UDI
Class IActive
ImmunoDNA Digestor 200 ml
FDA UDI
Class IActive
Helicobacter Pylori (EP279) BSB 3283 (ASR)
FDA UDI
Class IActive
Hematoxylin Counterstainer 15 ml
FDA UDI
Class IActive
Cytokeratin 8 & 18 RMab Concentrate, 1 ml
FDA UDI
Class IActive
CD23 control slides Control Slides, 5
FDA UDI
Class IActive
Mouse/Rabbit PolyDetector DAB HRP Brown Detection System 50 ml each
FDA UDI
Class IActive
Mohs ImmunoDigestor Ancillary, 100ml
FDA UDI
Class IActive
HER2 neu PolyDetector DAB HRP Brown Detection System 70 tests
FDA UDI
Class IActive
Tinto GLUT1 (RBT-GLUT1) BSB-3824-7
FDA UDI
Class IActive
p63 control slides Control Slides, 5
FDA UDI
Class IActive

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