Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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 78 of 111
DeviceModel / ReferenceRegistriesClassStatus
Helicobacter pylori, Polyclonal, RPab BSB 5608
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TLE1, BSB-142, MMab BSB-3784-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Mart-1|Melan-A, M2-7C10, MMab BSB 5752
EUDAMEDFDA UDI
IVD GeneralActive
Tinto LAG-3|CD223, EP294, RMab BSB 3364
EUDAMEDFDA UDI
IVD GeneralActive
Myeloperoxidase, Polyclonal, RPab BSB 5789
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Melanoma KBA.62, KBA.62, MMab BSB 6907
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Villin, CWWB1, MMab BSB 6015
EUDAMEDFDA UDI
IVD GeneralActive
Glycophorin A, GA-R2 (HIR2), MMab BSB 5587
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SOX-11, CL0142, MMab BSB 2217
EUDAMEDFDA UDI
IVD GeneralActive
LMO2, RBT-LM02, RMab BSB 3579
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgG4, BSB-96, MMab BSB 6808
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Glypican-3, 1G12, MMab BSB 6240
EUDAMEDFDA UDI
IVD GeneralActive
Villin, CWWB1, MMab BSB 6019
EUDAMEDFDA UDI
IVD GeneralActive
Tinto bcl-6, EP278, RMab BSB 2818
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgM, Polyclonal, RPab BSB 3081
EUDAMEDFDA UDI
IVD GeneralActive
CD74, LN2, MMab BSB 5300
EUDAMEDFDA UDI
IVD GeneralActive
TMPRSS2, BSB-136, MMab BSB-3703-01
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MTAP, RBT-MTAP, RMab BSB-3739-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ZFAND3, BSB-169, MMab BSB-3797-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgE, Polyclonal, RPab BSB 3069
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Albumin|FITC, polyclonal, RPab BSB-3000-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PD-1|CD279, EP239, RMab BSB 3150
EUDAMEDFDA UDI
IVD GeneralActive
MDM2, BSB-64, MMab BSB 2981
EUDAMEDFDA UDI
IVD GeneralActive
Glucagon, BSB-111, MMab BSB 3345
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CXCL12|SDF-1, BSB-165, MMab BSB-3713-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Glutamine Synthetase, GS-6, MMab BSB 2929
EUDAMEDFDA UDI
IVD GeneralActive
PD-L1|CD274, 28-8, RMab BSB-2371-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD56, 123C3.D5, MMab BSB 5268
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD38, EP135, RMab BSB 6499
EUDAMEDFDA UDI
IVD GeneralActive
MUC2, BSB-45, MMab BSB 6159
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Annexin A1, BSB-95, MMab BSB 6361
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgD, EP173, RMab BSB 2959
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Survivin, EP119, RMab BSB 2223
EUDAMEDFDA UDI
IVD GeneralActive
Tinto DOG-1, RBT-DOG1, RMab BSB 6270
EUDAMEDFDA UDI
IVD GeneralActive
Tinto B7H3|CD276, RBT-B7H3, RMab BSB 2810
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CXCL12|SDF-1, BSB-165, MMab BSB-3713-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto hGAL|GCET2, EP316, RMab BSB 2938
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD7, EP132, RMab BSB 2321
EUDAMEDFDA UDI
IVD GeneralActive
TIGIT, BSB-152, MMab BSB-3751-05
EUDAMEDFDA UDI
IVD GeneralActive
Mycobacterium tuberculosis, Polyclonal, RPab BSB 2996
EUDAMEDFDA UDI
IVD GeneralActive
LEF-1, EP310, RMab BSB 3381
EUDAMEDFDA UDI
IVD GeneralActive
Tinto INSM1, BSB-123, MMab BSB 3555
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD105|Endoglin, EP274, RMab BSB 2867
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MUC1, BSB-44, MMab BSB 6150
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast MiTF, C5 and D5, MMab BSB 3658
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SF-1|Steroidogenic Factor 1, BSB-149, MMab BSB-3746-3
EUDAMEDFDA UDI
IVD GeneralActive
NKX3.1, RM430, RMab BSB-3785-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Tau, BSB-115, MMab BSB 3427
EUDAMEDFDA UDI
IVD GeneralActive
CD79a, JCB117, MMab BSB 5307
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD147, BSB-137, MMab BSB-3704-3
EUDAMEDFDA UDI
IVD GeneralActive

Related Companies

Authorised Representatives

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.