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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 88 of 111
DeviceModel / ReferenceRegistriesClassStatus
CD56, 123C3.D5, MMab BSB 5272
EUDAMEDFDA UDI
IVD GeneralActive
CDK4, EP180, RMab BSB 2466
EUDAMEDFDA UDI
IVD GeneralActive
IgM, Polyclonal, RPab BSB 3084
EUDAMEDFDA UDI
IVD GeneralActive
p63, 4A4, MMab BSB 3605
EUDAMEDFDA UDI
IVD GeneralActive
CD45RO, UCHL-1, MMab BSB 5264
EUDAMEDFDA UDI
IVD GeneralActive
bcl-2, BSB-5, MMab BSB 5076
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Actin Smooth Muscle, BSB-15, MMab BSB 5030
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TCR Beta, BSB-117, MMab BSB 2260
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TCR Alpha, BSB-126, MMab BSB 3638
EUDAMEDFDA UDI
IVD GeneralActive
CD31, 1A10, MMab BSB 5223
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Progesterone Receptor, EP2, RMab BSB 2575
EUDAMEDFDA UDI
IVD GeneralActive
TIA-1, RBT-TIA1, RMab BSB-3782-05
EUDAMEDFDA UDI
IVD GeneralActive
YAP1, BSB-146, MMab BSB-3755-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto FGFR-3, BSB-150, MMab BSB-3724-15
EUDAMEDFDA UDI
IVD GeneralActive
HE4, EP370, RMab BSB 3352
EUDAMEDFDA UDI
IVD GeneralActive
DDR1, BSB-173, MMab BSB-3801-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p63, 4A4, MMab BSB 3602
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgA, BSB-39, MMab BSB 5659
EUDAMEDFDA UDI
IVD GeneralActive
Tinto HE4, EP370, RMab BSB 3351
EUDAMEDFDA UDI
IVD GeneralActive
CD138, B-A38, MMab BSB 5335
EUDAMEDFDA UDI
IVD GeneralActive
FOXP3, Polyclonal, RPab BSB 6761
EUDAMEDFDA UDI
IVD GeneralActive
Tinto HIF-1alpha, EP118, RMab BSB 2518
EUDAMEDFDA UDI
IVD GeneralActive
CD13, 38C12, MMab BSB 6328
EUDAMEDFDA UDI
IVD GeneralActive
Androgen Receptor, BSB-4, MMab BSB 6076
EUDAMEDFDA UDI
IVD GeneralActive
Estrogen Receptor, BSB-1, MMab BSB 2743
EUDAMEDFDA UDI
IVD GeneralActive
NKX2.2, EP336, RMab BSB 3110
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SATB2, EP281, RMab BSB 3199
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast Chromogranin A, LK2H10, MMab BSB-3773-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD25, RBT-CD25, RMab BSB 2455
EUDAMEDFDA UDI
IVD GeneralActive
Annexin VII, EP367, RMab BSB-3709-01
EUDAMEDFDA UDI
IVD GeneralActive
EMA, E29, MMab BSB 5482
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 19, BSB-34, MMab BSB 2737
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 8, EP17, RMab BSB 6662
EUDAMEDFDA UDI
IVD GeneralActive
Melanoma KBA.62, KBA.62, MMab BSB 6908
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p53, DO7, MMab BSB 5841
EUDAMEDFDA UDI
IVD GeneralActive
FOXP3, EP340, RMab BSB 2925
EUDAMEDFDA UDI
IVD GeneralActive
Claudin-1, Polyclonal, RPab BSB 6566
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD41| Integrin alpha IIb, EP178, RMab BSB 6506
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Thyroglobulin, 2H11 and 6E1, MMab BSB 2761
EUDAMEDFDA UDI
IVD GeneralActive
CD23, 1B12, MMab BSB 5209
EUDAMEDFDA UDI
IVD GeneralActive
Tinto HSP70, RM432, RMab BSB-3730-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD23, 1B12, MMab BSB 5205
EUDAMEDFDA UDI
IVD GeneralActive
Macrophage HAM-56, HAM-56, MMab BSB 5739
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Kappa|FITC, Polyclonal, GPab BSB-3009-3
EUDAMEDFDA UDI
IVD GeneralActive
Tyrosinase, BSB-6, MMab BSB 6012
EUDAMEDFDA UDI
IVD GeneralActive
CD56, 123C3.D5, MMab BSB 5270
EUDAMEDFDA UDI
IVD GeneralActive
GATA3, EP368, RMab BSB 3331
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast EpCAM, Ber-EP4, MMab BSB 3679
EUDAMEDFDA UDI
IVD GeneralActive
Tinto OCT-4, EP143, RMab BSB 2029
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Spectrin, RBC2|3D5, MMab BSB 5938
EUDAMEDFDA UDI
IVD GeneralActive

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