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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 41 of 111
DeviceModel / ReferenceRegistriesClassStatus
PolyDetector Liquid AEC HRP Red Ready-To-use, 500 ml
FDA UDI
Class IActive
Somatostatin control slides Control Slides, 5
FDA UDI
Class IActive
Histone H3 Phospho control slide Control Slides, 5
FDA UDI
Class IActive
CDX2 Control Slides Control Slides, 5
FDA UDI
Class IActive
TintoRetriever Digital Pressure Cooker Bundle BSB 7015
FDA UDI
Class IActive
PolyDetector HRP Black kit 500 Tests
FDA UDI
Class IActive
Insulin control slides Control Slides, 5
FDA UDI
Class IActive
Prolactin Control Slides BSB-9354-CS
FDA UDI
Class IActive
HER-2 neu (BSB-3) BSB 5635 (ASR)
FDA UDI
Class IActive
Tinto Calretinin (RBT-CALB2) BSB-3815-15
FDA UDI
Class IActive
Tinto PiT1 (BSB-182) BSB-3837-3
FDA UDI
Class IActive
S100p (rbt-S100p) BSB-3833-1
FDA UDI
Class IActive
CD19 control slides Control Slides, 5
FDA UDI
Class IActive
Mouse/Rabbit ImmunoDetector Biotin Link & AP Label Ready-to-use, 1000 ml each
FDA UDI
Class IActive
MiTF Control Slides BSB-9280-CS
FDA UDI
Class IActive
TintoRetriever Slide Thermometers BSB 7005
FDA UDI
Class IActive
Tinto HHV-8 (RBT-HHV8) BSB-3778-7-ASR
FDA UDI
Class IActive
IgE Control Slides BSB-9235-CS
FDA UDI
Class IActive
IDH1 R132H Control Slides BSB-9230-CS
FDA UDI
Class IActive
Cdx2 (rbt-Cdx2) BSB-3819-05
FDA UDI
Class IActive
PNI Carcinoma MultiDetector Detection System kit Ready-to-use, 70 tests each
FDA UDI
Class IActive
TintoCoverslips: 24mm x 40mm : 20 Packs of Precleaned Slides (20, 000 Total) BSB-7101-20000
FDA UDI
Class IActive
Langerin / CD207 RMab Concentrate, 1 ml
FDA UDI
Class IActive
Tinto Kappa, RPab Predilute, 15 ml
FDA UDI
Class IActive
S100A8/MRP8, RMab Concentrate, 0.1 ml
FDA UDI
Class IActive
TSH Control Slides BSB-9421-CS
FDA UDI
Class IActive
PDGFR-B Control Slides BSB-9340-CS
FDA UDI
Class IActive
Tinto CD19 (RM332) BSB-3840-15
FDA UDI
Class IActive
Kappa control slides Control Slides,5
FDA UDI
Class IActive
Tinto Cytokeratin 5, RMab Predilute, 3 ml
FDA UDI
Class IActive
HPV16 Control Slides Control Slides, 5
FDA UDI
Class IActive
TintoDetector 30-Well Ragent Holders BSB 7004
FDA UDI
Class IActive
IL-1b Control Slides BSB-9240-CS
FDA UDI
Class IActive
OX-40/CD134 control slides Control Slides, 5
FDA UDI
Class IActive
FluoroMounter with DAPI 1000 ml
FDA UDI
Class IActive
CD68 Control Slides BSB-9105-CS
FDA UDI
Class IActive
Tinto HER2 neu Phospho RMab Predilute, 7 ml
FDA UDI
Class IActive
c-Myc (RBT-CMYC) BSB-3813-01
FDA UDI
Class IActive
Progesterone Receptor (RBT-22) BSB 5886 (ASR)
FDA UDI
Class IActive
Tinto HHV-8 (RBT-HHV8) BSB-3778-15-ASR
FDA UDI
Class IActive
PELP1 Control Slides BSB-9342-CS
FDA UDI
Class IActive
Toxoplasma gondii (Polyclonal) BSB 6048 (ASR)
FDA UDI
Class IActive
CD45RA control slides Control Slides, 5
FDA UDI
Class IActive
Tinto Cytokeratin LMW AE1, MMab Predilute, 3 ml
FDA UDI
Class IActive
HEG1 Control Slides BSB-9204-CS
FDA UDI
Class IActive
COX-2 control slides Control Slides, 5
FDA UDI
Class IActive
MDM2 control slides Control Slides, 5
FDA UDI
Class IActive
Treponema pallidum (Polyclonal) BSB 3237 (ASR)
FDA UDI
Class IActive
Tinto c-Myc (RBT-CMYC) BSB-3813-7
FDA UDI
Class IActive
Neutrophil Elastase RMab Concentrate, 1 ml
FDA UDI
Class IActive

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