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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 84 of 111
DeviceModel / ReferenceRegistriesClassStatus
Tinto CD163, 10D6, MMab BSB 6304
EUDAMEDFDA UDI
IVD GeneralActive
MUC1, BSB-44, MMab BSB 6152
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p14 ARF, RBT-p14, RMab BSB 3596
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Pneumocystis jirovecii, 3F6, MMab BSB 5875
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cadherin17|LI-Cadherin, EP86, RMab BSB 6849
EUDAMEDFDA UDI
IVD GeneralActive
Tinto E-Cadherin, EP6, RMab BSB 5463
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 5 and 6, D5 and 16B4, MMab BSB 5403
EUDAMEDFDA UDI
IVD GeneralActive
MUC2, EP187, RMab BSB 6950
EUDAMEDFDA UDI
IVD GeneralActive
Caveolin-1, EP353, RMab BSB 3318
EUDAMEDFDA UDI
IVD GeneralActive
p16, RM267, RMab BSB-3768-1
EUDAMEDFDA UDI
IVD GeneralActive
PMS2, EP51, RMab BSB 2122
EUDAMEDFDA UDI
IVD GeneralActive
Calponin, BSB-20, MMab BSB 5125
EUDAMEDFDA UDI
IVD GeneralActive
MDR-1, JSB-1, MMab BSB 6903
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Uroplakin III, EP321, RMab BSB 3241
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Mart-1|Melan-A, A103, MMab BSB 6872
EUDAMEDFDA UDI
IVD GeneralActive
Tinto LH, BSB-53, MMab BSB 5723
EUDAMEDFDA UDI
IVD GeneralActive
HER2 neu, EP3, RMab BSB 2515
EUDAMEDFDA UDI
IVD GeneralActive
S100P, EP186, RMab BSB 2186
EUDAMEDFDA UDI
IVD GeneralActive
Treponema pallidum, Polyclonal, RPab BSB 3235
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD34, EP88, RMab BSB 6486
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Tyrosinase, BSB-6, MMab BSB 6008
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Actin Muscle Specific, HHF35, MMab BSB 5024
EUDAMEDFDA UDI
IVD GeneralActive
Claudin-7, EP399, RMab BSB-3719-01
EUDAMEDFDA UDI
IVD GeneralActive
ACTH, BSB-25, MMab BSB 5018
EUDAMEDFDA UDI
IVD GeneralActive
CD8, EP334, RMab BSB 2849
EUDAMEDFDA UDI
IVD GeneralActive
Myogenin, F5D, MMab BSB 5796
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TIA-1, TIA-1, MMab BSB 6352
EUDAMEDFDA UDI
IVD GeneralActive
HSP70, RM432, RMab BSB-3730-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgG|FITC, Polyclonal, GPab BSB-3007-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TFE3, EP285, RMab BSB 3227
EUDAMEDFDA UDI
IVD GeneralActive
Tinto C4c, Polyclonal, RPab BSB 3034
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MyoD1, EP212, RMab BSB 6974
EUDAMEDFDA UDI
IVD GeneralActive
Tinto GH, BSB-99, MMab BSB 3336
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Caldesmon, BSB-19, MMab BSB 6100
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MCM2, RBT-MCM2, RMab BSB 6333
EUDAMEDFDA UDI
IVD GeneralActive
GLUT1, EP141, RMab BSB 6782
EUDAMEDFDA UDI
IVD GeneralActive
CD147, BSB-137, MMab BSB-3704-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Factor H|Complement Factor H, BSB-164, MMab BSB-3723-3
EUDAMEDFDA UDI
IVD GeneralActive
INI-1, 25, MMab BSB 6832
EUDAMEDFDA UDI
IVD GeneralActive
NeuN, A60, MMab BSB 2010
EUDAMEDFDA UDI
IVD GeneralActive
CEA, BSB-13, MMab BSB 5340
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD5, RBT-CD5, RMab BSB 5157
EUDAMEDFDA UDI
IVD GeneralActive
PAX-7, BSB-145, MMab BSB-3743-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TCR Beta, BSB-117, MMab BSB 2259
EUDAMEDFDA UDI
IVD GeneralActive
p14 ARF, RBT-p14, RMab BSB 3599
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PHOX2B, EP312, RMab BSB 3609
EUDAMEDFDA UDI
IVD GeneralActive
COX-2, RBT-COX2, RMab BSB 5363
EUDAMEDFDA UDI
IVD GeneralActive
FOXP3, Polyclonal, RPab BSB 6763
EUDAMEDFDA UDI
IVD GeneralActive
Tinto STAR, EP226, RMab BSB 3631
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Myeloperoxidase, Polyclonal, RPab BSB 5787
EUDAMEDFDA UDI
IVD GeneralActive

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