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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 68 of 111
DeviceModel / ReferenceRegistriesClassStatus
CD44, BSB-12, MMab BSB 6237
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD75, LN-1, MMab BSB 2719
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Vimentin, V9, MMab BSB 6024
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SATB2, EP281, RMab BSB 3198
EUDAMEDFDA UDI
IVD GeneralActive
Amyloid Beta, RBT-A4, RMab BSB 3446
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TCR Delta, BSB-127, MMab BSB 3645
EUDAMEDFDA UDI
IVD GeneralActive
PAX-5, RBT-PAX5, RMab BSB 5865
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Mart-1|Melan-A, A103, MMab BSB 6871
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD11b, EP45, RMab BSB 6436
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CEA, Polyclonal, RPab BSB 6536
EUDAMEDFDA UDI
IVD GeneralActive
SV40, Pab101, MMab BSB 2234
EUDAMEDFDA UDI
IVD GeneralActive
Tinto HER-2 neu, BSB-3, MMab BSB 5633
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Mycobacterium tuberculosis, Polyclonal, RPab BSB 2992
EUDAMEDFDA UDI
IVD GeneralActive
Actin Muscle Specific, HHF35, MMab BSB 5027
EUDAMEDFDA UDI
IVD GeneralActive
C3c, Polyclonal, RPab BSB 3031
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MUC1, BSB-44, MMab BSB 6151
EUDAMEDFDA UDI
IVD GeneralActive
CD71, 10F11, MMab BSB 6525
EUDAMEDFDA UDI
IVD GeneralActive
Tinto EGFR, 31G7, MMab BSB 5471
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD45, 2B11 and PD7|26, MMab BSB 5248
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Macrophage HAM-56, HAM-56, MMab BSB 5738
EUDAMEDFDA UDI
IVD GeneralActive
Mammaglobin, EP249, RMab BSB 5747
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin HMW 34BE12, 34BetaE12, MMab BSB 5398
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Melanosome HMB45, HMB-45, MMab BSB 5757
EUDAMEDFDA UDI
IVD GeneralActive
E-Cadherin, EP6, RMab BSB 5466
EUDAMEDFDA UDI
IVD GeneralActive
CXCR5|CD185, Polyclonal, RPab BSB-3721-01
EUDAMEDFDA UDI
IVD GeneralActive
Mart-1|Melan-A, A103, MMab BSB 6875
EUDAMEDFDA UDI
IVD GeneralActive
Neurofilament, 2F11, MMab BSB 5818
EUDAMEDFDA UDI
IVD GeneralActive
CD79a, JCB117, MMab BSB 5306
EUDAMEDFDA UDI
IVD GeneralActive
Inhibin alpha, EP378, RMab BSB 3359
EUDAMEDFDA UDI
IVD GeneralActive
S-100, 4C4.9, MMab BSB 5920
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SS18-SSX, RBT-SS18-SSX, RMab BSB-3796-15
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast Podoplanin, D2-40, MMab BSB-3699-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TNFa-IP2, BSB-141, MMab BSB-3708-3
EUDAMEDFDA UDI
IVD GeneralActive
IFN-Gamma, BSB-161, MMab BSB-3734-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Ki-67, EP5, RMab BSB 5708
EUDAMEDFDA UDI
IVD GeneralActive
MCM3, EP202, RMab BSB 6887
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Villin, EP163, RMab BSB 2302
EUDAMEDFDA UDI
IVD GeneralActive
Tinto bcl-6, EP278, RMab BSB 2817
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MGMT|AGAT, EP337, RMab BSB-3737-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Myoglobin, EP87, RMab BSB 6982
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD99, BSB-9, MMab BSB 5309
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Thyroid Peroxidase, EP159, RMab BSB 2616
EUDAMEDFDA UDI
IVD GeneralActive
Lambda, BSB-16, MMab BSB 5720
EUDAMEDFDA UDI
IVD GeneralActive
p63, 4A4, MMab BSB 3607
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD8, C8|144B, MMab BSB 5170
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgE, Polyclonal, RPab BSB 3067
EUDAMEDFDA UDI
IVD GeneralActive
GH, EP267, RMab BSB 2500
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin Cocktail AE1 and AE3, AE1 and AE3, MMab BSB 5433
EUDAMEDFDA UDI
IVD GeneralActive
SMAD4|DPC4, BSB-63, MMab BSB 3207
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Nestin, EP287, RMab BSB 2001
EUDAMEDFDA UDI
IVD GeneralActive

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