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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 104 of 111
DeviceModel / ReferenceRegistriesClassStatus
Tinto INI-1, RBT-INI1, RMab BSB-3779-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto C1q|FITC, Polyclonal, RPab BSB-3001-3
EUDAMEDFDA UDI
IVD GeneralActive
Survivin, EP119, RMab BSB 2228
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Parvalbumin, EP300, RMab BSB 3408
EUDAMEDFDA UDI
IVD GeneralActive
IDH1 R132H, IHC132, MMab BSB 3549
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Ki-67, RM360, RMab BSB-3767-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD41| Integrin alpha IIb, EP178, RMab BSB 6508
EUDAMEDFDA UDI
IVD GeneralActive
p14 ARF, RBT-p14, RMab BSB 3598
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TCL1, EP105, RMab BSB 2252
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD45RA, 4KB5, MMab BSB 5254
EUDAMEDFDA UDI
IVD GeneralActive
CD35, RLB25, MMab BSB 5237
EUDAMEDFDA UDI
IVD GeneralActive
p120 Catenin, EP66, RMab BSB 2080
EUDAMEDFDA UDI
IVD GeneralActive
CD163, 10D6, MMab BSB 6306
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 20, Ks20.8, MMab BSB 5386
EUDAMEDFDA UDI
IVD GeneralActive
MUC1, EP85, RMab BSB 6943
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SALL4, 6E3, MMab BSB 3185
EUDAMEDFDA UDI
IVD GeneralActive
PAX-8, ZR-1, RMab BSB 2101
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast Ki-67, RM360, RMab BSB-3771-3
EUDAMEDFDA UDI
IVD GeneralActive
MNDA, BSB-157, MMab BSB-3738-1
EUDAMEDFDA UDI
IVD GeneralActive
CDK2, RBT-CDK2, RMab BSB 2640
EUDAMEDFDA UDI
IVD GeneralActive
Tri-Methyl-Histone H3(Lys27)|H3K27Me3, RBT-H3K27Me3, RMab BSB-3806-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin LMW CAM5.2, CAM5.2, MMab BSB 2057
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 18, EP30, RMab BSB 6697
EUDAMEDFDA UDI
IVD GeneralActive
CD35, RLB25, MMab BSB 5236
EUDAMEDFDA UDI
IVD GeneralActive
Tinto C3c, Polyclonal, RPab BSB 3027
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD73|NT5E, RM431, RMab BSB-3716-15
EUDAMEDFDA UDI
IVD GeneralActive
CD3, RBT-CD3, RMab BSB 6425
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD105|Endoglin, EP274, RMab BSB 2866
EUDAMEDFDA UDI
IVD GeneralActive
IFN-Gamma, BSB-161, MMab BSB-3734-01
EUDAMEDFDA UDI
IVD GeneralActive
Cyclin D1, RBT-14, RMab BSB 5370
EUDAMEDFDA UDI
IVD GeneralActive
Pneumocystis jirovecii, 3F6, MMab BSB 5878
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Glycophorin A, GA-R2 (HIR2), MMab BSB 5582
EUDAMEDFDA UDI
IVD GeneralActive
CD57, BSB-10, MMab BSB 5277
EUDAMEDFDA UDI
IVD GeneralActive
CD35, EP197, RMab BSB 6497
EUDAMEDFDA UDI
IVD GeneralActive
hPL, Polyclonal, RPab BSB 6803
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SMAD4|DPC4, RBT-SMAD4, RMab BSB 3400
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p16, RBT-p16, RMab BSB 3478
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MUC5AC, CLH2, MMab BSB 6165
EUDAMEDFDA UDI
IVD GeneralActive
Myoglobin, BSB-104, MMab BSB 3389
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Adipophilin|ADRP, BSB-91, MMab BSB 3247
EUDAMEDFDA UDI
IVD GeneralActive
SS18-SSX, RBT-SS18-SSX, RMab BSB-3796-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto C4d, EP272, RMab BSB 2833
EUDAMEDFDA UDI
IVD GeneralActive
CD4, RBT-CD4, RMab BSB 5152
EUDAMEDFDA UDI
IVD GeneralActive
Synaptophysin, Polyclonal, RPab BSB 5948
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Arginase-1, EP261, RMab BSB 2448
EUDAMEDFDA UDI
IVD GeneralActive
CD63, NKI|C3, MMab BSB 6300
EUDAMEDFDA UDI
IVD GeneralActive
TIM-3|HAVCR2|CD366, BSB-163, MMab BSB-3752-01
EUDAMEDFDA UDI
IVD GeneralActive
CEACAM7, BSB-168, MMab BSB-3791-05
EUDAMEDFDA UDI
IVD GeneralActive
MMP-9, EP127, RMab BSB 2543
EUDAMEDFDA UDI
IVD GeneralActive
Ksp-Cadherin, 4H6|F9, MMab BSB 6287
EUDAMEDFDA UDI
IVD GeneralActive

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