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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 87 of 111
DeviceModel / ReferenceRegistriesClassStatus
Tinto Fascin, BSB-36, MMab BSB 5514
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast NGFR, BSB-18, MMab BSB-3696-3
EUDAMEDFDA UDI
IVD GeneralActive
Helicobacter Pylori, EP279, RMab BSB 3284
EUDAMEDFDA UDI
IVD GeneralActive
Insulin, BSB-42, MMab BSB 5699
EUDAMEDFDA UDI
IVD GeneralActive
Tinto C3d, Polyclonal, RPab BSB 6389
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ATM, EP327, RMab BSB-3710-15
EUDAMEDFDA UDI
IVD GeneralActive
C4c, Polyclonal, RPab BSB 3036
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PLAP, BSB-47, MMab BSB 2756
EUDAMEDFDA UDI
IVD GeneralActive
TMPRSS2, BSB-136, MMab BSB-3703-1
EUDAMEDFDA UDI
IVD GeneralActive
CD117, RM359, RMab BSB-3758-05
EUDAMEDFDA UDI
IVD GeneralActive
Albumin, polyclonal, RPab BSB 3015
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PELP1, RBT-PELP1, RMab BSB-3744-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TRAcP, 9C5, MMab BSB 5982
EUDAMEDFDA UDI
IVD GeneralActive
CTLA-4|CD152, BSB-88, MMab BSB 2884
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TAG-72, BSB-21, MMab BSB 5952
EUDAMEDFDA UDI
IVD GeneralActive
Zap-70, 2F3.2, MMab BSB 6040
EUDAMEDFDA UDI
IVD GeneralActive
S100P, EP186, RMab BSB 2185
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD33, RBT-CD33, RMab BSB 3449
EUDAMEDFDA UDI
IVD GeneralActive
CD45, 2B11 and PD7|26, MMab BSB 5251
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MTAP, RBT-MTAP, RMab BSB-3739-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Pygopus 2|Pygo 2, BSB-156, MMab BSB-3745-3
EUDAMEDFDA UDI
IVD GeneralActive
CD8, EP334, RMab BSB 2848
EUDAMEDFDA UDI
IVD GeneralActive
PDX1, EP139, RMab BSB 3158
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Claudin-1, Polyclonal, RPab BSB 6563
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p120 Catenin, EP66, RMab BSB 2077
EUDAMEDFDA UDI
IVD GeneralActive
Lambda|FITC, Polyclonal, GPab BSB-3010-1
EUDAMEDFDA UDI
IVD GeneralActive
Pneumocystis jirovecii, 3F6, MMab BSB 5880
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p16, RBT-p16, RMab BSB 3476
EUDAMEDFDA UDI
IVD GeneralActive
ACTH, BSB-25, MMab BSB 5020
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PD-L1|CD274, 28-8, RMab BSB-2371-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SALL4, EP299, RMab BSB 3191
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgM, BSB-41, MMab BSB 5682
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cyclin B1, RM281, RMab BSB-3760-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto c-Met|HGFR, EP1454Y, RMab BSB 6583
EUDAMEDFDA UDI
IVD GeneralActive
CD14, 7, MMab BSB 6315
EUDAMEDFDA UDI
IVD GeneralActive
CD63, NKI|C3, MMab BSB 6301
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Nestin, EP287, RMab BSB 2002
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 20, Ks20.8, MMab BSB 5387
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Uroplakin III, Polyclonal, RPab BSB 2288
EUDAMEDFDA UDI
IVD GeneralActive
SOX-9, EP317, RMab BSB 3216
EUDAMEDFDA UDI
IVD GeneralActive
Trop-2|EGP-1, BSB-148, MMab BSB-3754-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TSH, EP254, RMab BSB 2622
EUDAMEDFDA UDI
IVD GeneralActive
CD142|TF|Coagulation Factor III, BSB-143, MMab BSB-3718-1
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 35BH11, 35BetaH11, MMab BSB 5425
EUDAMEDFDA UDI
IVD GeneralActive
NGFR, BSB-18, MMab BSB 6294
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TIGIT, BSB-152, MMab BSB-3751-7
EUDAMEDFDA UDI
IVD GeneralActive
IL-1a, BSB-138, MMab BSB-3705-01
EUDAMEDFDA UDI
IVD GeneralActive
CD142|TF|Coagulation Factor III, BSB-143, MMab BSB-3718-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Parafibromin, BSB-50, MMab BSB 2748
EUDAMEDFDA UDI
IVD GeneralActive
CD7, EP132, RMab BSB 2326
EUDAMEDFDA UDI
IVD GeneralActive

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