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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 75 of 111
DeviceModel / ReferenceRegistriesClassStatus
MiTF, C5 and D5, MMab BSB 6250
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD16, EP364, RMab BSB 3322
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Vimentin, V9, MMab BSB 6023
EUDAMEDFDA UDI
IVD GeneralActive
TLE1, RBT-TLE1, RMab BSB-3794-1
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast Adipophilin, BSB-91, MMab BSB-3772-7
EUDAMEDFDA UDI
IVD GeneralActive
ZFAND3, BSB-169, MMab BSB-3797-01
EUDAMEDFDA UDI
IVD GeneralActive
Tinto NGFR, BSB-18, MMab BSB 6289
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD5, RBT-CD5, RMab BSB 5156
EUDAMEDFDA UDI
IVD GeneralActive
Fascin, BSB-36, MMab BSB 5517
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast Synaptophysin, Polyclonal, RPab BSB-3775-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Spectrin, RBC2|3D5, MMab BSB 5940
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ACE2, BSB-135, MMab BSB-3702-3
EUDAMEDFDA UDI
IVD GeneralActive
Estrogen Receptor, RM292, RMab BSB-3765-01
EUDAMED
IVD GeneralActive
Tinto CD99, BSB-9, MMab BSB 5311
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD1a, EP80, RMab BSB 5136
EUDAMEDFDA UDI
IVD GeneralActive
HER-2 neu, RBT-HER2, RMab BSB 2039
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ACTH, BSB-25, MMab BSB 5015
EUDAMEDFDA UDI
IVD GeneralActive
STAT6, EP325, RMab BSB 3425
EUDAMEDFDA UDI
IVD GeneralActive
Tinto DDR1, BSB-173, MMab BSB-3801-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD14, EP128, RMab BSB 6457
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MLH1, G168-728, MMab BSB 5764
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MDR-1, JSB-1, MMab BSB 6899
EUDAMEDFDA UDI
IVD GeneralActive
LAG-3|CD223, EP294, RMab BSB 3367
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CEA, Polyclonal, RPab BSB 6535
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p21, DCS-60.2, MMab BSB 2064
EUDAMEDFDA UDI
IVD GeneralActive
Calcitonin, EP92, RMab BSB 6411
EUDAMEDFDA UDI
IVD GeneralActive
CD117, EP10, RMab BSB 5321
EUDAMEDFDA UDI
IVD GeneralActive
CD7, LP15, MMab BSB 5165
EUDAMEDFDA UDI
IVD GeneralActive
Tinto A-1-Antitrypsin, Polyclonal, RPab BSB 5009
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Podoplanin|D2-40, D2-40, MMab BSB 6065
EUDAMEDFDA UDI
IVD GeneralActive
GH, BSB-99, MMab BSB 3338
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 20, EP23, RMab BSB 6706
EUDAMEDFDA UDI
IVD GeneralActive
Ki-67, RM360, RMab BSB-3767-01
EUDAMEDFDA UDI
IVD GeneralActive
CD138, B-A38, MMab BSB 5333
EUDAMEDFDA UDI
IVD GeneralActive
CD38, SPC32, MMab BSB 6203
EUDAMEDFDA UDI
IVD GeneralActive
Collagen Type IV, CIV22, MMab BSB 5356
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD3, RBT-CD3, RMab BSB 6422
EUDAMEDFDA UDI
IVD GeneralActive
C4c, Polyclonal, RPab BSB 3038
EUDAMEDFDA UDI
IVD GeneralActive
CD19, BSB-97, MMab BSB 6229
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD7, EP132, RMab BSB 2323
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TSH, BSB-56, MMab BSB 5996
EUDAMEDFDA UDI
IVD GeneralActive
Tinto hPL, Polyclonal, RPab BSB 6801
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Neurofilament, 2F11, MMab BSB 5814
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TTF-1, 8G7G3|1, MMab BSB 6003
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Amyloid Beta, RBT-A4, RMab BSB 3441
EUDAMEDFDA UDI
IVD GeneralActive
Tinto APOE4, BSB-170, MMab BSB-3798-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD137|TNFRSF9, BSB-159, MMab BSB-3717-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD7, EP132, RMab BSB 2322
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Fibrinogen, Polyclonal, RPab BSB 3047
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Somatostatin Receptor 2|SSTR2, EP149, RMab BSB-3748-15
EUDAMEDFDA UDI
IVD GeneralActive

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