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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 70 of 111
DeviceModel / ReferenceRegistriesClassStatus
Tinto MUC1, EP85, RMab BSB 6941
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TIGIT, BSB-152, MMab BSB-3751-15
EUDAMEDFDA UDI
IVD GeneralActive
CD74, LN2, MMab BSB 5298
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Collagen Type IV, CIV22, MMab BSB 5352
EUDAMEDFDA UDI
IVD GeneralActive
Tinto C1q, Polyclonal, RPab BSB 3020
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Uroplakin III, EP321, RMab BSB 3240
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD71, 10F11, MMab BSB 6522
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 4, EP4, RMab BSB 6594
EUDAMEDFDA UDI
IVD GeneralActive
Tinto GAB1|GRB2-associated-binding protein 1, BSB-155, MMab BSB-3727-7
EUDAMEDFDA UDI
IVD GeneralActive
OCT-2, EP115, RMab BSB 2024
EUDAMEDFDA UDI
IVD GeneralActive
INSM1, BSB-123, MMab BSB 3558
EUDAMEDFDA UDI
IVD GeneralActive
CD103|ITGAE, EP206, RMab BSB 2864
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 7, OV-TL 12|30, MMab BSB 5408
EUDAMEDFDA UDI
IVD GeneralActive
PAX-5, RBT-PAX5, RMab BSB 5866
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast CK AE1 and AE3, AE1 and AE3, MMab BSB 3664
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD23, EP75, RMab BSB 6472
EUDAMEDFDA UDI
IVD GeneralActive
Claudin-1, Polyclonal, RPab BSB 6565
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Histone H3 Phospho, EP233, RMab BSB 2526
EUDAMEDFDA UDI
IVD GeneralActive
Tinto c-Myc, EP121, RMab BSB 6577
EUDAMEDFDA UDI
IVD GeneralActive
HPV16, CAMVIR-1, MMab BSB 2947
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD45RA, 4KB5, MMab BSB 5255
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CA19-9, 121SLE, MMab BSB 5106
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Herpes Simplex Virus II, BSB-116, MMab BSB 3464
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PTEN, RBT-PTEN, RMab BSB 2644
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Zap-70, 2F3.2, MMab BSB 6038
EUDAMEDFDA UDI
IVD GeneralActive
Claudin-1, Polyclonal, RPab BSB 6567
EUDAMEDFDA UDI
IVD GeneralActive
Helicobacter pylori, Polyclonal, RPab BSB 5607
EUDAMEDFDA UDI
IVD GeneralActive
Glutamine Synthetase, GS-6, MMab BSB 2934
EUDAMEDFDA UDI
IVD GeneralActive
Macrophage HAM-56, HAM-56, MMab BSB 5741
EUDAMEDFDA UDI
IVD GeneralActive
IgG, BSB-40, MMab BSB 5676
EUDAMEDFDA UDI
IVD GeneralActive
Napsin A, BSB-112, MMab BSB 3397
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MTAP, RBT-MTAP, RMab BSB-3739-15
EUDAMEDFDA UDI
IVD GeneralActive
ZFAND3, BSB-169, MMab BSB-3797-05
EUDAMEDFDA UDI
IVD GeneralActive
FOXP3, Polyclonal, RPab BSB 6762
EUDAMEDFDA UDI
IVD GeneralActive
Lysozyme, EP134, RMab BSB 6860
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Lamin-B1, RBT-LMNB1, RMab BSB-3735-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD5, RM314, RMab BSB-3759-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Aurora B, RM278, RMab BSB-3712-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto hPL, EP241, RMab BSB 2412
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TCR Delta, BSB-127, MMab BSB 3644
EUDAMEDFDA UDI
IVD GeneralActive
PHOX2B, EP312, RMab BSB 3612
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 20, Ks20.8, MMab BSB 5389
EUDAMEDFDA UDI
IVD GeneralActive
p63, EP174, RMab BSB 5853
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p21, DCS-60.2, MMab BSB 2065
EUDAMEDFDA UDI
IVD GeneralActive
C1q|FITC, Polyclonal, RPab BSB-3001-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD61, EP65, RMab BSB 3512
EUDAMEDFDA UDI
IVD GeneralActive
Survivin, EP119, RMab BSB 2226
EUDAMEDFDA UDI
IVD GeneralActive
C3d, Polyclonal, RPab BSB 6392
EUDAMEDFDA UDI
IVD GeneralActive
Tinto APOE4, BSB-170, MMab BSB-3798-15
EUDAMEDFDA UDI
IVD GeneralActive
Somatostatin, BSB-113, MMab BSB 3416
EUDAMEDFDA UDI
IVD GeneralActive

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