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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 15 of 111
DeviceModel / ReferenceRegistriesClassStatus
Insulin Control Slides BSB-9247-CS
FDA UDI
Class IActive
Granzyme B Control Slides BSB-9201-CS
FDA UDI
Class IActive
Mouse/Rabbit AmpliDetector Plus FITC with FluoroMounter with DAPI BSB-0358-50
FDA UDI
Class IActive
Adipophilin / ADRP control slides Control Slides, 5
FDA UDI
Class IActive
PTEN MMab Concentrate, 0.1 ml
FDA UDI
Class IActive
Slide Holder BSB 7010
FDA UDI
Class IActive
Tinto Toxoplasma gondii , RPab Predilute, 15 ml
FDA UDI
Class IActive
CD4 Control Slides Control Slides, 5
FDA UDI
Class IActive
Mouse/Rabbit PolyDetector Plus Link & HRP Label Ready-to-use, 200 ml each
FDA UDI
Class IActive
Vimentin Control Slides BSB-9428-CS
FDA UDI
Class IActive
Cd19 (rm332) BSB-3840-05
FDA UDI
Class IActive
Herpes Simplex Virus I (Polyclonal) BSB 2430 (ASR)
FDA UDI
Class IActive
Cytokeratin 14 RMab Concentrate, 1 ml
FDA UDI
Class IActive
INSM1 control slides Control Slides, 5
FDA UDI
Class IActive
Tinto Spectrin, RMab Predilute, 3 ml
FDA UDI
Class IActive
Tinto SATB2 (RBT-SATB2) BSB-3848-15
FDA UDI
Class IActive
INI-1 Control Slides BSB-9244-CS
FDA UDI
Class IActive
TintoFast CK CAM5.2 MMab Predilute, 15ml
FDA UDI
Class IActive
ATRX Control Slides BSB-9022-CS
FDA UDI
Class IActive
PolyDetector Peroxidase Blocker 100 ml
FDA UDI
Class IActive
Treponema TMA, Artificial (2-core: Positive and Negative) Control Slides Control Slides, 5
FDA UDI
Class IActive
Tinto Insulin, RMab Predilute, 7 ml
FDA UDI
Class IActive
Cytokeratin 5 & 6 control slides Control Slides, 5
FDA UDI
Class IActive
Parvovirus (R92F6) BSB 5859 (ASR)
FDA UDI
Class IActive
ImmunoDetector Biotin Blocker 1000 ml
FDA UDI
Class IActive
Myogenin Control Slides BSB-9298-CS
FDA UDI
Class IActive
Tinto COX-2, RMab Predilute, 3 ml
FDA UDI
Class IActive
Tinto Treponema pallidum (Polyclonal) BSB 3233 (ASR)
FDA UDI
Class IActive
Parvovirus (R92F6) BSB 5857 (ASR)
FDA UDI
Class IActive
MSH6 Control Slides BSB-9285-CS
FDA UDI
Class IActive
SV40 (Pab101) BSB 2234 (ASR)
FDA UDI
Class IActive
Lysozyme RPab Concentrate, 0.1 ml
FDA UDI
Class IActive
Tinto Prolactin (RBT-PRL) BSB-3845-7
FDA UDI
Class IActive
CD56 control slides Control Slides, 5
FDA UDI
Class IActive
Pd-L1/Cd274 (28-8) BSB-2371-1-ASR
FDA UDI
Class IActive
CD63 Control Slides BSB-9104-CS
FDA UDI
Class IActive
Mouse/Rabbit ImmunoDetector AP, w/ALK Scarlet Detection System 200 ml each (2000 tests)
FDA UDI
Class IActive
Tinto HPV (BSB-66) BSB 5653 (ASR)
FDA UDI
Class IActive
Mouse/Rabbit ImmunoDetector DAB HRP Brown Detection System 15 ml each
FDA UDI
Class IActive
Tinto Herpes Simplex Virus II (Polyclonal) BSB 2336 (ASR)
FDA UDI
Class IActive
Tinto SOX-2, RMab Predilute 15 ml
FDA UDI
Class IActive
Tinto EGFR (31G7) BSB 5471 (ASR)
FDA UDI
Class IActive
BCOR Control Slides Control Slides, 5
FDA UDI
Class IActive
Tinto Cyclin D, 1 RMab Predilute, 3 ml
FDA UDI
Class IActive
CD163 control slides Control Slides, 5
FDA UDI
Class IActive
INSM1 control slides Control Slides, 5
FDA UDI
Class IActive
Tinto Treponema pallidum (Polyclonal) BSB 3234 (ASR)
FDA UDI
Class IActive
Tinto PSA RMab Predilute, 15 ml
FDA UDI
Class IActive
CITED1 Control Slides BSB-9446-CS
FDA UDI
Class IActive
ROS-1 Control Slides BSB-9365-CS
FDA UDI
Class IActive

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