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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 106 of 111
DeviceModel / ReferenceRegistriesClassStatus
Tinto Caveolin-1, EP353, RMab BSB 3315
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Kappa|FITC, Polyclonal, GPab BSB-3009-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Progesterone Receptor, RBT-22, RMab BSB 5884
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Lambda, BSB-16, MMab BSB 5717
EUDAMEDFDA UDI
IVD GeneralActive
bcl-6, EP278, RMab BSB 2821
EUDAMEDFDA UDI
IVD GeneralActive
TdT, EP266, RMab BSB 2613
EUDAMEDFDA UDI
IVD GeneralActive
pan-TRK, RBT-TRK, RMab BSB-2376-1
EUDAMEDFDA UDI
IVD GeneralActive
HHV-8, 13B10, MMab BSB 5648
EUDAMEDFDA UDI
IVD GeneralActive
Tinto NKX2.2, EP336, RMab BSB 3107
EUDAMEDFDA UDI
IVD GeneralActive
BRG-1|SMARCA4, BSB-154, MMab BSB-3714-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Laminin-R|RPSA, BSB-144, MMab BSB-3736-15
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast CK 5 and 6, D5 and 16B4, MMab BSB 3667
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IFN-Gamma, BSB-161, MMab BSB-3734-7
EUDAMEDFDA UDI
IVD GeneralActive
Collagen Type IV, RBT-COL4, RMab BSB-3777-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Mammaglobin, EP249, RMab BSB 5745
EUDAMEDFDA UDI
IVD GeneralActive
HER2 neu, EP3, RMab BSB 2514
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast SOX-10, BSB-62, MMab BSB 3656
EUDAMEDFDA UDI
IVD GeneralActive
SALL4, EP299, RMab BSB 3195
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CEA, Polyclonal, RPab BSB 6534
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Nanog, EP225, RMab BSB 3581
EUDAMEDFDA UDI
IVD GeneralActive
PGP 9.5, BSB-46, MMab BSB 2117
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Thyroglobulin, BSB-49, MMab BSB 5975
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TCR Beta, BSB-117, MMab BSB 2258
EUDAMEDFDA UDI
IVD GeneralActive
ACTH, BSB-25, MMab BSB 5019
EUDAMEDFDA UDI
IVD GeneralActive
Tinto HE4, EP370, RMab BSB 3350
EUDAMEDFDA UDI
IVD GeneralActive
CA15-3, DF3, MMab BSB 5102
EUDAMEDFDA UDI
IVD GeneralActive
APOE4, BSB-170, MMab BSB-3798-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Epstein Barr Virus LMP-1, CS1-4, MMab BSB 5485
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Parathyroid Hormone| PTH, BSB-24, MMab BSB 2085
EUDAMEDFDA UDI
IVD GeneralActive
TCL1, EP105, RMab BSB 2254
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PD-1|CD279, EP239, RMab BSB 3149
EUDAMEDFDA UDI
IVD GeneralActive
SALL4, EP299, RMab BSB 3194
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Melanoma PNL2, PNL2, MMab BSB 6914
EUDAMEDFDA UDI
IVD GeneralActive
BCA-225, Cu-18, MMab BSB 5068
EUDAMEDFDA UDI
IVD GeneralActive
Somatostatin, BSB-113, MMab BSB 3418
EUDAMEDFDA UDI
IVD GeneralActive
PAX-7, BSB-145, MMab BSB-3743-1
EUDAMEDFDA UDI
IVD GeneralActive
GCDFP-15, 23A3, MMab BSB 5559
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD71, 10F11, MMab BSB 6521
EUDAMEDFDA UDI
IVD GeneralActive
Musashi 2, RM422, RMab BSB-3740-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Melanoma PNL2, PNL2, MMab BSB 6913
EUDAMEDFDA UDI
IVD GeneralActive
Alpha-Fetoprotein, BSB-23, MMab BSB 5053
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin MNF116, MNF116, MMab BSB 3536
EUDAMEDFDA UDI
IVD GeneralActive
Tinto LEF-1, EP310, RMab BSB 3378
EUDAMEDFDA UDI
IVD GeneralActive
Tinto GH, BSB-99, MMab BSB 3335
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ERG, EP111, RMab BSB 6738
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Topoisomerase IIa, RBT-Topo2a, RMab BSB 6338
EUDAMEDFDA UDI
IVD GeneralActive
Tinto DDR1, BSB-173, MMab BSB-3801-15
EUDAMEDFDA UDI
IVD GeneralActive
Chromogranin A, LK2H10, MMab BSB 5348
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD44, BSB-12, MMab BSB 6234
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Thymidylate synthase|TS, BSB-160, MMab BSB-3750-15
EUDAMEDFDA UDI
IVD GeneralActive

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