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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 91 of 111
DeviceModel / ReferenceRegistriesClassStatus
MGMT|AGAT, EP337, RMab BSB-3737-01
EUDAMEDFDA UDI
IVD GeneralActive
PMS2, EP51, RMab BSB 2124
EUDAMEDFDA UDI
IVD GeneralActive
LRG1, BSB-174, MMab BSB-3802-1
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast Melanoma Cocktail: HMB-45, Mart-1 and Tyrosinase, HMB-45, A103 and BSB-6, MMab BSB-3695-15
EUDAMEDFDA UDI
IVD GeneralActive
COX-2, RBT-COX2, RMab BSB 5361
EUDAMEDFDA UDI
IVD GeneralActive
A-1-Antitrypsin, Polyclonal, RPab BSB 5011
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Gastrin, Polyclonal, RPab BSB 5549
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD23, 1B12, MMab BSB 5204
EUDAMEDFDA UDI
IVD GeneralActive
TSH, BSB-56, MMab BSB 5998
EUDAMEDFDA UDI
IVD GeneralActive
OX-40|CD134, BSB-90, MMab BSB 3124
EUDAMEDFDA UDI
IVD GeneralActive
CTLA-4|CD152, RBT-CTLA-4, RMab BSB 3486
EUDAMEDFDA UDI
IVD GeneralActive
TLE1, 1F5, MMab BSB 2317
EUDAMEDFDA UDI
IVD GeneralActive
CD123 IL-3Ra, BSB-59, MMab BSB 5326
EUDAMEDFDA UDI
IVD GeneralActive
YAP1, BSB-146, MMab BSB-3755-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto EpCAM|Epithelial Specific Antigen, MOC-31, MMab BSB 6725
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin MNF116, MNF116, MMab BSB 3534
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IFN-Gamma, BSB-161, MMab BSB-3734-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto C3d, Polyclonal, RPab BSB 6388
EUDAMEDFDA UDI
IVD GeneralActive
Cyclin D1, RM241, RMab BSB-3761-1
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin OSCAR, OSCAR, MMab BSB 6180
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ACTH, BSB-25, MMab BSB 5017
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD4, RBT-CD4, RMab BSB 5149
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Laminin-R|RPSA, BSB-144, MMab BSB-3736-3
EUDAMEDFDA UDI
IVD GeneralActive
SOX-11, CL0142, MMab BSB 2219
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TLE1, RBT-TLE1, RMab BSB-3794-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto NKX3.1, RM430, RMab BSB-3785-7
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 8 and 18, B22.1 and B23.1, MMab BSB 5419
EUDAMEDFDA UDI
IVD GeneralActive
CD11c, EP157, RMab BSB 6446
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD35, EP197, RMab BSB 6494
EUDAMEDFDA UDI
IVD GeneralActive
Tinto EGFR, 31G7, MMab BSB 5470
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 19, BSB-34, MMab BSB 2733
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Herpes Simplex Virus I and II, 10A3 and BSB-116, MMab BSB 3471
EUDAMED
IVD GeneralActive
Thymidylate synthase|TS, BSB-160, MMab BSB-3750-05
EUDAMEDFDA UDI
IVD GeneralActive
CD14, 7, MMab BSB 6313
EUDAMEDFDA UDI
IVD GeneralActive
Tinto BRAF V600E, RM8, RMab BSB 2824
EUDAMEDFDA UDI
IVD GeneralActive
MiTF, C5 and D5, MMab BSB 6252
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD21, EP64, RMab BSB 5199
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Fli-1, G146-222, MMab BSB 5519
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TORC3|CRTC3, BSB-175, MMab BSB-3805-7
EUDAMEDFDA UDI
IVD GeneralActive
GCDFP-15, 23A3, MMab BSB 5557
EUDAMEDFDA UDI
IVD GeneralActive
Langerin, 12D6, MMab BSB 6847
EUDAMEDFDA UDI
IVD GeneralActive
STAT6, EP325, RMab BSB 3424
EUDAMEDFDA UDI
IVD GeneralActive
CDK4, EP180, RMab BSB 2464
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD38, EP135, RMab BSB 6501
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD138, EP201, RMab BSB 6528
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Estrogen Receptor, RM292, RMab BSB-3765-3
EUDAMED
IVD GeneralActive
Spectrin, RBC2|3D5, MMab BSB 5942
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD61, 2f2, MMab BSB 5282
EUDAMEDFDA UDI
IVD GeneralActive
Tinto C3c, Polyclonal, RPab BSB 3026
EUDAMEDFDA UDI
IVD GeneralActive
Tinto WT1, 6F-H2, MMab BSB 6031
EUDAMEDFDA UDI
IVD GeneralActive

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