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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 16 of 111
DeviceModel / ReferenceRegistriesClassStatus
CD13 RMab Concentrate, 1 ml
FDA UDI
Class IActive
HSP-27 MMab Concentrate, 1 ml
FDA UDI
Class IActive
Tinto CD15, RMab Predilute, 15 ml
FDA UDI
Class IActive
Spectrin Control Slides BSB-9387-CS
FDA UDI
Class IActive
ImmunoDetector Protein Blocker / Antibody Diluent 200 ml
FDA UDI
Class IActive
Lef1 (rbt-Lef1) BSB-3826-05
FDA UDI
Class IActive
Tinto Progesterone Receptor (RBT-22) BSB 5882 (ASR)
FDA UDI
Class IActive
Rabbit FluoroDetector FITC with FluoroMounter with DAPI 100 ml
FDA UDI
Class IActive
Tinto MDR-1 RMab Predilute, 15 ml
FDA UDI
Class IActive
Ezh2 (rbt-Ezh2) BSB-3823-05
FDA UDI
Class IActive
Mouse/Rabbit PolyDetector HRP Label Ready-to-use, 50 ml each
FDA UDI
Class IActive
FluoroMounter 15 ml
FDA UDI
Class IActive
Tinto MyoD1 (RBT-MYOD1) BSB-3829-7
FDA UDI
Class IActive
PNI Carcinoma MultiDetector (CK 5 & 6 Cocktail & NGFR) BSB-0353-50
FDA UDI
Class IActive
Methyl Green Counterstainer 200 ml
FDA UDI
Class IActive
Tinto IgD RPab Predilute, 7 ml
FDA UDI
Class IActive
Tinto Bcl-x RMab Predilute, 3 ml
FDA UDI
Class IActive
Fascin Control Slides Control Slides, 5
FDA UDI
Class IActive
Cadherin-6, RMab Concentrate, 1 ml
FDA UDI
Class IActive
Tinto CD10 RMab Predilute, 15 ml
FDA UDI
Class IActive
Cytokeratin 14 control slides Control Slides, 5
FDA UDI
Class IActive
Histone H3 Phospho (RBT-pHH3) BSB-3844-01
FDA UDI
Class IActive
Calcitonin (RBT-Calcitonin) BSB-3814-01
FDA UDI
Class IActive
Fibrinogen / FITC control slides control slides, 5
FDA UDI
Class IActive
SATB2 control slides Control Slides, 5
FDA UDI
Class IActive
Hepatitis B Virus Surface Antigen MMab Concentrate, 1 ml
FDA UDI
Class IActive
IgG Control Slides BSB-9236-CS
FDA UDI
Class IActive
Tinto Hepatitis B Virus Surface Antigen (A10F1) BSB 5617 (ASR)
FDA UDI
Class IActive
Progesterone Receptor (EP2) BSB 2576 (ASR)
FDA UDI
Class IActive
TintoDeparaffinator EDTA 20X 1000 ml
FDA UDI
Class IActive
TNFa-IP2 Control Slides BSB-9414-CS
FDA UDI
Class IActive
PAX-2 Control Slides BSB-9333-CS
FDA UDI
Class IActive
Adipophilin/ADRP Control Slides BSB-9007-CS
FDA UDI
Class IActive
Cyclin B1 control slides Control Slides, 5
FDA UDI
Class IActive
Mouse/Rabbit PolyDetector DAB HRP Brown Detection System 200 ml each
FDA UDI
Class IActive
Immuno/DNA Washer 10X 1 Lt
FDA UDI
Class IActive
Granzyme B RPab Concentrate, 1 ml
FDA UDI
Class IActive
Mouse/Rabbit ImmunoDetector AEC HRP Red 1000ml
FDA UDI
Class IActive
PolyDetector Liquid DAB HRP Brown kit 150 Tests
FDA UDI
Class IActive
S100a8/Mrp8 (rbt-Mrp8) BSB-3847-05
FDA UDI
Class IActive
PLA2R1 Control Slides Control Slides, 5
FDA UDI
Class IActive
CD13 RMab Concentrate, 0.1 ml
FDA UDI
Class IActive
Progesterone Receptor (BSB-2) BSB 2129 (ASR)
FDA UDI
Class IActive
TintoReagent Container 30mL BSB-7457
FDA UDI
Class IActive
Tinto BAP1 (RBT-BAP1) BSB-3839-15
FDA UDI
Class IActive
Hepatitis B Virus Core Antigen control slides Control Slides, 5
FDA UDI
Class IActive
TintoStainer Plus Automated System LX BSB-7400-60
FDA UDI
Class IActive
Epstein Barr Virus LMP-1 Control Slides Control Slides, 5
FDA UDI
Class IActive
Bax control slides Control Slides, 5
FDA UDI
Class IActive
PTEN Control Slides BSB-9360-CS
FDA UDI
Class IActive

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