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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 94 of 111
DeviceModel / ReferenceRegistriesClassStatus
Tinto HEG1, SKM9-2, MMab BSB-3728-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgG, BSB-40, MMab BSB 5675
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Adipophilin|ADRP, BSB-91, MMab BSB 3246
EUDAMEDFDA UDI
IVD GeneralActive
bcl-6, EP278, RMab BSB 2820
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Galectin-3, 9C4, MMab BSB 5542
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD30, Ber-H2, MMab BSB 5212
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Glypican-3, 1G12, MMab BSB 6241
EUDAMEDFDA UDI
IVD GeneralActive
Beta-Catenin, 14, MMab BSB 5089
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast HMB-45, HMB-45, MMab BSB-3693-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PLAP, BSB-47, MMab BSB 2754
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CEA, BSB-13, MMab BSB 5338
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ERCC1, EP219, RMab BSB 2484
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgG4, BSB-96, MMab BSB 6809
EUDAMEDFDA UDI
IVD GeneralActive
Fumarate Hydratase|Fumarase, BSB-151, MMab BSB-3726-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Stathmin, EP247, RMab BSB 2594
EUDAMEDFDA UDI
IVD GeneralActive
Kappa Light Chains, BSB-58, MMab BSB 5704
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TDP-43|TARDBP, BSB-166, MMab BSB-3776-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IL-6, BSB-140, MMab BSB-3707-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Melanoma PNL2, PNL2, MMab BSB 6912
EUDAMEDFDA UDI
IVD GeneralActive
Parvalbumin, EP300, RMab BSB 3410
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TIM-3|HAVCR2|CD366, BSB-163, MMab BSB-3752-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Prolactin, EP193, RMab BSB 2133
EUDAMEDFDA UDI
IVD GeneralActive
Tinto FSH, BSB-55, MMab BSB 5533
EUDAMEDFDA UDI
IVD GeneralActive
STAT6, EP325, RMab BSB 3423
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Estrogen Receptor, EP1, RMab BSB 2491
EUDAMEDFDA UDI
IVD GeneralActive
ACE2, BSB-135, MMab BSB-3702-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD19, BSB-97, MMab BSB 6226
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 19, RM364, RMab BSB-3763-05
EUDAMEDFDA UDI
IVD GeneralActive
NeuN, A60, MMab BSB 2012
EUDAMEDFDA UDI
IVD GeneralActive
p27, SX53G8, MMab BSB 5838
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Chromogranin A, LK2H10, MMab BSB 5344
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ICOS|CD278, RM417, RMab BSB-3731-7
EUDAMEDFDA UDI
IVD GeneralActive
Adipophilin|ADRP, BSB-91, MMab BSB 3249
EUDAMEDFDA UDI
IVD GeneralActive
CD75, LN-1, MMab BSB 2724
EUDAMEDFDA UDI
IVD GeneralActive
MTAP, RBT-MTAP, RMab BSB-3739-1
EUDAMEDFDA UDI
IVD GeneralActive
bcl-6, RBT-bcl6, RMab BSB 5081
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 8 and 18, B22.1 and B23.1, MMab BSB 5415
EUDAMEDFDA UDI
IVD GeneralActive
CD34, QBEnd|10, MMab BSB 5230
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Beta-Catenin, RM276, RMab BSB-3756-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MUC-4, EP256, RMab BSB 2554
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin OSCAR, OSCAR, MMab BSB 6182
EUDAMEDFDA UDI
IVD GeneralActive
Tinto BRG-1|SMARCA4, BSB-154, MMab BSB-3714-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PD-1|CD279, EP239, RMab BSB 3148
EUDAMEDFDA UDI
IVD GeneralActive
Gastrin, Polyclonal, RPab BSB 5551
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD8, EP334, RMab BSB 2846
EUDAMEDFDA UDI
IVD GeneralActive
p27, SX53G8, MMab BSB 5837
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 17, BSB-33, MMab BSB 2730
EUDAMEDFDA UDI
IVD GeneralActive
Glucagon, BSB-111, MMab BSB 3347
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CA15-3, DF3, MMab BSB 5101
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Napsin A, RBT-NAPSA, RMab BSB-3789-15
EUDAMEDFDA UDI
IVD GeneralActive

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