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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 73 of 111
DeviceModel / ReferenceRegistriesClassStatus
Islet 1|ISL1, EP283, RMab BSB 2974
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 7, RM284, RMab BSB-3764-15
EUDAMEDFDA UDI
IVD GeneralActive
IgM| FITC, Polyclonal, RPab BSB-3008-1
EUDAMEDFDA UDI
IVD GeneralActive
MDM2, BSB-64, MMab BSB 2983
EUDAMEDFDA UDI
IVD GeneralActive
INSM1, BSB-123, MMab BSB 3557
EUDAMEDFDA UDI
IVD GeneralActive
Macrophage HAM-56, HAM-56, MMab BSB 5740
EUDAMEDFDA UDI
IVD GeneralActive
TRAcP, 9C5, MMab BSB 5985
EUDAMEDFDA UDI
IVD GeneralActive
Claudin-4, EP417, RMab BSB-3792-05
EUDAMEDFDA UDI
IVD GeneralActive
CD16, EP364, RMab BSB 3325
EUDAMEDFDA UDI
IVD GeneralActive
Topoisomerase IIa, RBT-Topo2a, RMab BSB 6341
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Parathyroid Hormone| PTH, BSB-24, MMab BSB 2084
EUDAMEDFDA UDI
IVD GeneralActive
CD2, AB75, MMab BSB 6210
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p40, ZR8, RMab BSB 2071
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TCR Alpha, BSB-126, MMab BSB 3637
EUDAMEDFDA UDI
IVD GeneralActive
TNFa-IP2, BSB-141, MMab BSB-3708-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto GATA3, L50-823, MMab BSB 2670
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 20, Ks20.8, MMab BSB 5390
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Prealbumin|Transthyretin, BSB-125, MMab BSB 3618
EUDAMEDFDA UDI
IVD GeneralActive
Progesterone Receptor, EP2, RMab BSB 2576
EUDAMEDFDA UDI
IVD GeneralActive
Vimentin, EP21, RMab BSB 2310
EUDAMEDFDA UDI
IVD GeneralActive
Inhibin alpha, EP378, RMab BSB 3360
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast CD34, QBEnd|10, MMab BSB 3683
EUDAMEDFDA UDI
IVD GeneralActive
ATRX, BSB-108, MMab BSB 3298
EUDAMEDFDA UDI
IVD GeneralActive
MSH2, RBT-MSH2, RMab BSB 6931
EUDAMEDFDA UDI
IVD GeneralActive
CD30, Ber-H2, MMab BSB 5214
EUDAMEDFDA UDI
IVD GeneralActive
Tinto BRG-1|SMARCA4, BSB-154, MMab BSB-3714-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CA-125, OC125, MMab BSB 5093
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 19, BSB-34, MMab BSB 2734
EUDAMEDFDA UDI
IVD GeneralActive
WT1, 6F-H2, MMab BSB 6033
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD7, LP15, MMab BSB 5164
EUDAMEDFDA UDI
IVD GeneralActive
Renal Cell Carcinoma, PN-15, MMab BSB 5913
EUDAMEDFDA UDI
IVD GeneralActive
Tinto LRG1, BSB-174, MMab BSB-3802-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD20, L26, MMab BSB 5192
EUDAMEDFDA UDI
IVD GeneralActive
CD2, AB75, MMab BSB 6209
EUDAMEDFDA UDI
IVD GeneralActive
Tinto AMACRacemase|P504S, 13H4, RMab BSB 5058
EUDAMEDFDA UDI
IVD GeneralActive
ROS-1, EP282, RMab BSB 3627
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 14, RM328, RMab BSB-3762-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Myogenin, F5D, MMab BSB 5793
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast CK AE1 and AE3, AE1 and AE3, MMab BSB 3663
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TTF-1, 8G7G3|1, MMab BSB 6002
EUDAMEDFDA UDI
IVD GeneralActive
Tinto INI-1, RBT-INI1, RMab BSB-3779-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin MNF116, MNF116, MMab BSB 3532
EUDAMEDFDA UDI
IVD GeneralActive
Beta-Catenin, RM276, RMab BSB-3756-01
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TFE3, EP285, RMab BSB 3225
EUDAMEDFDA UDI
IVD GeneralActive
CDK2, RBT-CDK2, RMab BSB 2641
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD1a, EP80, RMab BSB 5135
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Fumarate Hydratase|Fumarase, BSB-151, MMab BSB-3726-3
EUDAMEDFDA UDI
IVD GeneralActive
pTau Phospho|Thr 181, BSB-176, MMab BSB-3807-1
EUDAMEDFDA UDI
IVD GeneralActive
Beta-Catenin, 14, MMab BSB 5088
EUDAMEDFDA UDI
IVD GeneralActive
S100A1, EP184, RMab BSB 2165
EUDAMEDFDA UDI
IVD GeneralActive

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