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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 25 of 111
DeviceModel / ReferenceRegistriesClassStatus
Cd19 (rm332) BSB-3840-01
FDA UDI
Class IActive
NKX2.2 Control Slides BSB-9308-CS
FDA UDI
Class IActive
Cytokeratin 13 RMab Concentrate, 1 ml
FDA UDI
Class IActive
Tinto Candida Albicans (RBT-C.alb) BSB-3803-3-ASR
FDA UDI
Class IActive
PSP94/MSMB, RMab Concentrate, 0.5 ml
FDA UDI
Class IActive
Tinto Estrogen Receptor (BSB-1) BSB 2742 (ASR)
FDA UDI
Class IActive
Tinto HLA-DR alpha chain RMab Predilute, 7 ml
FDA UDI
Class IActive
Helicobacter Pylori (EP279) BSB 3282 (ASR)
FDA UDI
Class IActive
Estrogen Receptor (EP1) BSB 2494 (ASR)
FDA UDI
Class IActive
PolyDetector HRP Green kit 5000 Tests
FDA UDI
Class IActive
PolyDetector HRP Black BSB-0361-50
FDA UDI
Class IActive
Synaptophysin Control Slides BSB-9394-CS
FDA UDI
Class IActive
Desmin control slides Control Slides, 5
FDA UDI
Class IActive
GCDFP-15 Control Slides BSB-9193-CS
FDA UDI
Class IActive
SOX-11 Control Slides BSB-9383-CS
FDA UDI
Class IActive
Herpes Simplex Virus I (10A3) BSB 2687 (ASR)
FDA UDI
Class IActive
MMP-9 Control Slides BSB-9282-CS
FDA UDI
Class IActive
Tinto Pneumocystis jirovecii (3F6) BSB 5877 (ASR)
FDA UDI
Class IActive
Tinto PiT1 (BSB-182) BSB-3837-15
FDA UDI
Class IActive
Tinto FOXA1 / HNF-3A, RPab Predilute, 3ml
FDA UDI
Class IActive
CD38 control slides Control Slides, 5
FDA UDI
Class IActive
Tinto Hepatitis B Virus Core Antigen RPab Concentrate, 0.5 ml
FDA UDI
Class IActive
CD163 control slides Control Slides, 5
FDA UDI
Class IActive
Tinto T. cruzi (BSB-183) BSB-3838-3-ASR
FDA UDI
Class IActive
Thyroglobulin RMab Concentrate, 0.5 ml
FDA UDI
Class IActive
Mouse/Rabbit PolyDetector HRP Label Ready-to-use, 200 ml each
FDA UDI
Class IActive
Thyroglobulin Control Slides Control Slides, 5
FDA UDI
Class IActive
Hpv (bsb-66) BSB 5655 (ASR)
FDA UDI
Class IActive
Tinto HPV (BSB-66) BSB 5652 (ASR)
FDA UDI
Class IActive
Mouse/Rabbit PolyDetector AEC HRP Red Detection System 200 ml each
FDA UDI
Class IActive
CD19 Control Slides BSB-9075-CS
FDA UDI
Class IActive
PolyDetector Alk Brown Ready-To-Use 100 ml,
FDA UDI
Class IActive
Alpha-Fetoprotein RMab Concentrate, 0.1 ml
FDA UDI
Class IActive
CD10 control slides Control Slides, 5
FDA UDI
Class IActive
ChromoProtector 50 ml
FDA UDI
Class IActive
Somatostatin RMab Concentrate, 1 ml
FDA UDI
Class IActive
Mohs Mouse/Rabbit PolyDetector HRP Green Detection System Kit, 50ml
FDA UDI
Class IActive
Tinto CD10 (RBT-CD10) BSB-3816-7
FDA UDI
Class IActive
Tinto SOX-11 (BSB-167) BSB-3783-3
FDA UDI
Class IActive
Cytokeratin 18 control slides Control Slides, 5
FDA UDI
Class IActive
Toxoplasma gondii RPab Concentrate, 0.1 ml
FDA UDI
Class IActive
Langerin / CD207 RMab Concentrate, 0.1 ml
FDA UDI
Class IActive
Melanoma Cocktail: HMB-45 Mart-1 & Tyrosinase control slides Control Slides, 5
FDA UDI
Class IActive
CD35 control slides Control Slides, 5
FDA UDI
Class IActive
MUC4 Control Slides BSB-9289-CS
FDA UDI
Class IActive
Progesterone Receptor (EP2) BSB 2577 (ASR)
FDA UDI
Class IActive
OLIG2 Control Slides BSB-9316-CS
FDA UDI
Class IActive
MCM2 control slides Control Slides, 5
FDA UDI
Class IActive
Glutamine Synthetase Control Slides Control Slides, 5
FDA UDI
Class IActive
Cadherin-6 , RMab Concentrate, 0.5 ml
FDA UDI
Class IActive

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