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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 76 of 111
DeviceModel / ReferenceRegistriesClassStatus
IFN-Alpha, BSB-158, MMab BSB-3733-01
EUDAMEDFDA UDI
IVD GeneralActive
Ki-67, RM360, RMab BSB-3767-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Stathmin, EP247, RMab BSB 2595
EUDAMEDFDA UDI
IVD GeneralActive
PD-L1|CD274, RBT-PDL1, RMab BSB 2653
EUDAMEDFDA UDI
IVD GeneralActive
PTEN, RBT-PTEN, RMab BSB 2646
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgE|FITC, Polyclonal, GPab BSB-3011-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Arginase-1, EP261, RMab BSB 2449
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Amyloid A, EP335, RMab BSB 2803
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IL-1a, BSB-138, MMab BSB-3705-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cyclin D3, BSB-171, MMab BSB-3799-3
EUDAMEDFDA UDI
IVD GeneralActive
HER-2 neu, RBT-HER2, RMab BSB 2038
EUDAMEDFDA UDI
IVD GeneralActive
CD61, 2f2, MMab BSB 5284
EUDAMEDFDA UDI
IVD GeneralActive
EpCAM|Epithelial Specific Antigen, MOC-31, MMab BSB 6727
EUDAMEDFDA UDI
IVD GeneralActive
DDR1, BSB-173, MMab BSB-3801-1
EUDAMEDFDA UDI
IVD GeneralActive
BRG-1|SMARCA4, BSB-154, MMab BSB-3714-01
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Mesothelial Cell, HBME-1, MMab BSB 3456
EUDAMEDFDA UDI
IVD GeneralActive
IgA, BSB-39, MMab BSB 5664
EUDAMEDFDA UDI
IVD GeneralActive
YAP1, BSB-146, MMab BSB-3755-01
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Progesterone Receptor, EP2, RMab BSB 2574
EUDAMEDFDA UDI
IVD GeneralActive
Albumin|FITC, polyclonal, RPab BSB-3000-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD117, EP10, RMab BSB 5316
EUDAMEDFDA UDI
IVD GeneralActive
Albumin|FITC, polyclonal, RPab BSB-3000-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MSH6, 44, MMab BSB 6142
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Myelin Basic Protein, EP207, RMab BSB 6960
EUDAMEDFDA UDI
IVD GeneralActive
Tinto LRG1, BSB-174, MMab BSB-3802-15
EUDAMEDFDA UDI
IVD GeneralActive
CXCL12|SDF-1, BSB-165, MMab BSB-3713-05
EUDAMEDFDA UDI
IVD GeneralActive
Herpes Simplex Virus I, 10A3, MMab BSB 2689
EUDAMEDFDA UDI
IVD GeneralActive
CXCL12|SDF-1, BSB-165, MMab BSB-3713-01
EUDAMEDFDA UDI
IVD GeneralActive
TNFa-IP2, BSB-141, MMab BSB-3708-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IDH1 R132H, RBT-IDH1, RMab BSB-3732-7
EUDAMEDFDA UDI
IVD GeneralActive
HHV-8, 13B10, MMab BSB 5650
EUDAMEDFDA UDI
IVD GeneralActive
Fibrinogen, Polyclonal, RPab BSB 3050
EUDAMEDFDA UDI
IVD GeneralActive
hGAL|GCET2, EP316, RMab BSB 2939
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Prolactin, EP193, RMab BSB 2135
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin LMW CAM5.2, CAM5.2, MMab BSB 2061
EUDAMEDFDA UDI
IVD GeneralActive
HE4, EP370, RMab BSB 3354
EUDAMEDFDA UDI
IVD GeneralActive
CD105|Endoglin, EP274, RMab BSB 2869
EUDAMEDFDA UDI
IVD GeneralActive
NKX2.2, EP336, RMab BSB 3111
EUDAMEDFDA UDI
IVD GeneralActive
Galectin-3, 9C4, MMab BSB 5544
EUDAMEDFDA UDI
IVD GeneralActive
p63, EP174, RMab BSB 5851
EUDAMEDFDA UDI
IVD GeneralActive
Zap-70, 2F3.2, MMab BSB 6039
EUDAMEDFDA UDI
IVD GeneralActive
MUC-4, EP256, RMab BSB 2556
EUDAMEDFDA UDI
IVD GeneralActive
Herpes Simplex Virus II, BSB-116, MMab BSB 3466
EUDAMEDFDA UDI
IVD GeneralActive
Caldesmon, BSB-19, MMab BSB 6102
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 7, RM284, RMab BSB-3764-05
EUDAMEDFDA UDI
IVD GeneralActive
PGP 9.5, BSB-46, MMab BSB 2116
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 17, BSB-33, MMab BSB 2726
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Herpes Simplex Virus II, BSB-116, MMab BSB 3463
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MCM3, EP202, RMab BSB 6884
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Brachyury, RBT-TBXT, RMab BSB 3492
EUDAMEDFDA UDI
IVD GeneralActive

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