Consumer Technology Association
UnclaimedIndustry
Electrical/Electronic Manufacturing
Staff
360
HQ
1919 S Eads St, Arlington, Virginia
Phone
+1 866-858-1555
Website
cta.techEngagement overview
Consumer Technology Association has filed 187 public comments across 165 dockets at 27 federal agencies, most actively at the Federal Trade Commission.
187
Comments filed
165
Dockets engaged
27
Agencies
Jul 14, 2026
Last filing
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Agency footprint
Dockets · FDA (13)
sorted by most recent filingFDANonrulemakingFDA-2024-D-4488
Artificial Intelligence-Enabled Device Software Functions: Lifecycle Management and Marketing Submission Recommendations; Draft Guidance for Industry and Food and Drug Administration Staff; Availability
1 of your filingslast filed Apr 8, 20254 co-filers
FDANonrulemakingFDA-2024-D-4689
Considerations for the Use of Artificial Intelligence to Support Regulatory Decision-Making for Drug and Biological Products; Draft Guidance for Industry; Availability; Agency Information Collection Activities; Proposed Collection; Comment Request
1 of your filingslast filed Apr 8, 202532 co-filers
FDANonrulemakingFDA-2022-D-2628
Marketing Submission Recommendations for a Modification Control Plan for Artificial Intelligence/Machine Learning (AI/ML)-Enabled Device Software Functions; Draft Guidance for Industry and Food and Drug Administration Staff; Availability
1 of your filingslast filed Jul 5, 20233 co-filers
FDANonrulemakingFDA-2021-D-1128
Digital Health Technologies for Remote Data Acquisition in Clinical Investigations; Draft Guidance for Industry, Investigators, and Other Stakeholders; Availability
1 of your filingslast filed Mar 28, 20221 co-filers
FDANonrulemakingFDA-2021-N-0555
Medical Devices; Ear, Nose, and Throat Devices; Establishing Over-the-Counter Hearing Aids and Aligning Other Regulations
1 of your filingslast filed Jan 20, 202261 co-filers
FDANonrulemakingFDA-2020-N-1933
Communicating Cybersecurity Vulnerabilities to Patients: Considerations for a Framework
1 of your filingslast filed Dec 22, 20201 co-filers
FDANonrulemakingFDA-2017-D-6569
Clinical and Patient Decision Support Software
2 of your filingslast filed Jan 2, 20203 co-filers
FDANonrulemakingFDA-2019-N-1185
Proposed Regulatory Framework for Modifications to Artificial Intelligence/Machine Learning (AI/ML)-Based Software as a Medical Device (SaMD) - Discussion Paper and Request for Feedback
1 of your filingslast filed Jun 7, 20193 co-filers
FDANonrulemakingFDA-2017-N-4301
Fostering Medical Innovation: A Plan for Digital Health Devices; Software Precertification Pilot Program
3 of your filingslast filed Jul 18, 20183 co-filers
FDANonrulemakingFDA-2018-N-1910
Fulfillment of 21st Century Cures Act Section 3060 Required Report
1 of your filingslast filed Jul 18, 201813 co-filers
FDANonrulemakingFDA-2018-D-1339
Multiple Function Software Device Products: Policy and Considerations
1 of your filingslast filed Jul 6, 20182 co-filers
FDANonrulemakingFDA-2017-D-6294
Changes to Existing Medical Software Policies Resulting from Section 3060 of the 21st Century Cures Act; Draft Guidance for Industry and Food and Drug Administration Staff; Availability
1 of your filingslast filed Feb 8, 20182 co-filers
FDANonrulemakingFDA-2013-D-1295
Regulatory Requirements for Hearing Aid Devices and Personal Sound Amplification Products; Draft Guidance for Industry and Food and Drug Administration Staff; Availability
1 of your filingslast filed May 18, 20161 co-filers
Attribution is name-based and imperfect. Firmographic data is third-party sourced and shown for demonstration. regulations.gov data is public record.