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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 107 of 111
DeviceModel / ReferenceRegistriesClassStatus
Tinto Tryptase, G3, MMab BSB 5987
EUDAMEDFDA UDI
IVD GeneralActive
Spectrin, RBC2|3D5, MMab BSB 5943
EUDAMEDFDA UDI
IVD GeneralActive
Tinto HSP70, RM432, RMab BSB-3730-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD105|Endoglin, EP274, RMab BSB 2868
EUDAMEDFDA UDI
IVD GeneralActive
CITED1, BSB-177, MMab BSB-3808-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Inhibin alpha, EP378, RMab BSB 3356
EUDAMEDFDA UDI
IVD GeneralActive
Stathmin, EP247, RMab BSB 2599
EUDAMEDFDA UDI
IVD GeneralActive
Tinto FSH, EP257, RMab BSB 3541
EUDAMEDFDA UDI
IVD GeneralActive
Melanoma PNL2, PNL2, MMab BSB 6915
EUDAMEDFDA UDI
IVD GeneralActive
Inhibin Alpha, R1, MMab BSB 5690
EUDAMEDFDA UDI
IVD GeneralActive
Tau, BSB-115, MMab BSB 3432
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TdT, EP266, RMab BSB 2610
EUDAMEDFDA UDI
IVD GeneralActive
MUC2, BSB-45, MMab BSB 6160
EUDAMEDFDA UDI
IVD GeneralActive
C1q|FITC, Polyclonal, RPab BSB-3001-1
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 5 and 6, D5 and 16B4, MMab BSB 5405
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TIM-3|HAVCR2|CD366, BSB-163, MMab BSB-3752-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Nestin, EP287, RMab BSB 2000
EUDAMEDFDA UDI
IVD GeneralActive
Galectin-3, 9C4, MMab BSB 5545
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SATB2, EP281, RMab BSB 3197
EUDAMEDFDA UDI
IVD GeneralActive
Parafibromin, BSB-50, MMab BSB 2752
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Neurofilament, EP79, RMab BSB 2014
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD5, RBT-CD5, RMab BSB 5155
EUDAMEDFDA UDI
IVD GeneralActive
COX-2, RBT-COX2, RMab BSB 5362
EUDAMEDFDA UDI
IVD GeneralActive
CD6, BSB-54, MMab BSB 2710
EUDAMEDFDA UDI
IVD GeneralActive
Parvalbumin, EP300, RMab BSB 3409
EUDAMEDFDA UDI
IVD GeneralActive
Retinoblastoma| Rb, 1F8, MMab BSB 6132
EUDAMEDFDA UDI
IVD GeneralActive
Estrogen Receptor, EP1, RMab BSB 2493
EUDAMEDFDA UDI
IVD GeneralActive
Tinto A-1-Antichymotrypsin, EP384, RMab BSB 3497
EUDAMEDFDA UDI
IVD GeneralActive
EGFR, 31G7, MMab BSB 5473
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MyoD1, EP212, RMab BSB 6975
EUDAMEDFDA UDI
IVD GeneralActive
CD7, LP15, MMab BSB 5166
EUDAMEDFDA UDI
IVD GeneralActive
p27, SX53G8, MMab BSB 5839
EUDAMEDFDA UDI
IVD GeneralActive
IL-1a, BSB-138, MMab BSB-3705-05
EUDAMEDFDA UDI
IVD GeneralActive
Estrogen Receptor, RBT-11, RMab BSB 5494
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD13, 38C12, MMab BSB 6325
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MUC2, EP187, RMab BSB 6946
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Claudin-4, EP417, RMab BSB-3792-7
EUDAMEDFDA UDI
IVD GeneralActive
HPV, BSB-66, MMab BSB 5655
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Trop-2|EGP-1, BSB-148, MMab BSB-3754-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Progesterone Receptor, BSB-2, MMab BSB 2127
EUDAMEDFDA UDI
IVD GeneralActive
Annexin A1, BSB-95, MMab BSB 6364
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TNFa-IP2, BSB-141, MMab BSB-3708-7
EUDAMEDFDA UDI
IVD GeneralActive
Osteonectin|SPARC, BSB-93, MMab BSB 3261
EUDAMEDFDA UDI
IVD GeneralActive
Tinto pan-TRK, RBT-TRK, RMab BSB-2376-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IMP-3|1GF2BP3, EP286, RMab BSB 2964
EUDAMEDFDA UDI
IVD GeneralActive
Melanoma KBA.62, KBA.62, MMab BSB 6909
EUDAMEDFDA UDI
IVD GeneralActive
Tinto GFAP, G-A-5, MMab BSB 5563
EUDAMEDFDA UDI
IVD GeneralActive
bcl-10, BSB-22, MMab BSB 2701
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD34, QBEnd|10, MMab BSB 5225
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MLH1, RBT-MLH1, RMab BSB-3787-15
EUDAMEDFDA UDI
IVD GeneralActive

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