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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 9 of 111
DeviceModel / ReferenceRegistriesClassStatus
GLUT1 Control Slides BSB-9197-CS
FDA UDI
Class IActive
Mouse/Rabbit ImmunoDetector AP Label Ready-to-use, 1000 ml
FDA UDI
Class IActive
CD7 Control Slides BSB-9106-CS
FDA UDI
Class IActive
CDK2 Control Slides BSB-9114-CS
FDA UDI
Class IActive
Tinto Parvovirus (R92F6) BSB 5855 (ASR)
FDA UDI
Class IActive
Mouse/Rabbit ImmunoDetector AP Label Ready-to-use, 100 ml
FDA UDI
Class IActive
Ctla-4/Cd152 (bsb-88) BSB 2885 (ASR)
FDA UDI
Class IActive
Mouse/Rabbit AmpliDetector Plus FITC BSB-0359-50
FDA UDI
Class IActive
Tinto Tryptase, RMab Predilute, 7 ml
FDA UDI
Class IUnknown
PolyDetector Liquid AEC HRP Red Ready-To-Use, 50 ml
FDA UDI
Class IActive
Tinto PAX-6 RMab Predilute, 3 ml
FDA UDI
Class IActive
PolyDetector Alk Blue Ready-To-Use 100 ml
FDA UDI
Class IActive
Tinto CTLA-4/CD152 (BSB-88) BSB 2882 (ASR)
FDA UDI
Class IActive
Oct4/Pou5f1 (rbt-Oct4) BSB-3830-1
FDA UDI
Class IActive
OCT-4 Control Slides BSB-9315-CS
FDA UDI
Class IActive
IgD Control Slides BSB-9234-CS
FDA UDI
Class IActive
Cytokeratin 13 RMab Concentrate, 0.5 ml
FDA UDI
Class IActive
Clusterin/ Apolipoprotein J RMab Concentrate, 0.1 ml
FDA UDI
Class IActive
Tinto Detector Complete System BSB 7000
FDA UDI
Class IActive
Mouse/Rabbit AmpliDetector Plus FITC with FluoroMounter BSB-0357-100
FDA UDI
Class IActive
Varicella Zoster Virus MMab Concentrate, 0.1 ml
FDA UDI
Class IActive
Amyloid A control slides Control Slides, 5
FDA UDI
Class IActive
PSAP RMab Concentrate, 0.5 ml
FDA UDI
Class IActive
PolyDetector HRP Blue kit 150 Tests
FDA UDI
Class IActive
Tff3 (bsb-181) BSB-3820-1
FDA UDI
Class IActive
5-core BRAF V600E Cell Line Microarray Control Slides Control Slides, 5
FDA UDI
Class IActive
Cytokeratin 8 & 18 Control Slides BSB-9152-CS
FDA UDI
Class IActive
CTLA-4/CD152 control slides Control Slides, 5
FDA UDI
Class IActive
CD23 control slides Control Slides, 5
FDA UDI
Class IActive
TintoDetector Staining System BSB 7001
FDA UDI
Class IActive
PolyDetector Alk Scarlet 50 ml
FDA UDI
Class IActive
Tinto Cytokeratin 14, RMab Predilute, 3 ml
FDA UDI
Class IActive
Methyl Green Counterstainer 50 ml
FDA UDI
Class IActive
pan-TRK (RM423) BSB-3742-05-ASR
FDA UDI
Class IActive
Tinto Neutrophil Elastase, RMab Predilute, 7 ml
FDA UDI
Class IActive
MyoD1 Control Slides BSB-9297-CS
FDA UDI
Class IActive
Tinto Cytokeratin 7, RMab Predilute, 7 ml
FDA UDI
Class IActive
Mart-1/Melan A Control Slides Control Slides, 5
FDA UDI
Class IActive
CD5 RMab Control Slides Control Slides, 5
FDA UDI
Class IActive
Glypican-3 control slides Control Slides, 5
FDA UDI
Class IActive
HER-2 neu (RBT-HER2) BSB 2039 (ASR)
FDA UDI
Class IActive
S100P Control Slides Control Slides, 5
FDA UDI
Class IActive
Tinto S100 Beta, RMab Predilute, 7 ml
FDA UDI
Class IActive
PDX1 Control Slides BSB-9341-CS
FDA UDI
Class IActive
PolyDetector Alk Magenta 15 ml
FDA UDI
Class IActive
Tinto SV40 (Pab101) BSB 2232 (ASR)
FDA UDI
Class IActive
Tinto PSAP, RMab Predilute, 7 ml
FDA UDI
Class IActive
bcl-10 Control Slides BSB-9028-CS
FDA UDI
Class IActive
Tinto Myelin Basic Protein, RMab Predilute, 7 ml
FDA UDI
Class IActive
SV-40 Cell Line Array (2-core: Positive and Negative) Control Slides Control Slides, 5
FDA UDI
Class IActive

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