AFFINITY BIOSENSORS

FDA Device Registration & Listing · Santa Barbara, CA, US · Registration 3025772277

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3025772277
FEI Number
3025772277
Entity Name
AFFINITY BIOSENSORS
City/State/Country
Santa Barbara, CA, US
Establishment Address
222 E Canon Perdido St Ste 101, Santa Barbara, CA 93101, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Affinity Biosensors (Owner Number: 10091217)
Owner / Operator Contact Address
222 E Canon Perdido Street, Suite 101, Santa Barbara, CA 93101, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

LifeScale Gram Negative Kit (LSGN) with the LifeScale AST system

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LON System, Test, Automated, Antimicrobial Susceptibility, Short Incubation Microbiology Class 2 866.1645 2024-07-25
SAN Automated Antimicrobial Susceptibility Test System For Positive Blood Culture Samples Microbiology Class 2 866.1650 2024-07-25

Official Correspondent

Ken Babcock

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Affinity Biosensors
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K033458 Becton, Dickinson & CO BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM - CONFIRMATORY ESBL TEST 2004-05-28
K112000 bioMerieux, Inc. VITEK 2 STREPTOCOCCUS PENICILLIN 2011-10-26

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0170-2015 Siemens Healthcare Diagnostics, Inc. 2
Rapid Neg BP Combo Panel Type 3; Catalog number B 1017-117. MicroScan Rapid panels are designed for use in determining identification to the species level and/or antimicrobial agent susceptibility of rapidly growing aerobic and facultatively anaerobic gram negative bacilli.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3025772277. Last updated year: 2026. Please use registration number 3025772277 when referencing this establishment in official correspondence.
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