Data / Medical devices / United States / Active Protective Technologies, Inc.
Active Protective Technologies, Inc.: FDA-registered device maker in Conshohocken, PA, United States, 1 510(k) clearance
Active Protective Technologies, Inc. is registered with the FDA (registration 3038206342) in Conshohocken, PA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 9, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3038206342
- Address
- 1100 E Hector St Ste 223, Conshohocken, PA, United States, 19428
- Owner or operator
- Active Protective Technologies, Inc. (10093404)
- Roles
- Complaint file establishment, Manufacturer, Repackager or relabeler, Reprocessor, Specification developer
- First device listed
- May 12, 2025
- Registered through
- 2026
- Brand names listed
- Tango Belt, Tango Belt Connectivity Device
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Medical Device Data System | OUG | 1 | Complaint file establishment, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Wearable Fall Injury Prevention Device | SEC | 2 | Complaint file establishment, Repackager or relabeler, Reprocessor, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 9, 2025 | DEN240021 | Tango® Belt (Model SAS-001-01 (XS); Model SAS-001-02 (S); Model SAS-001-03 (M); Model SAS-001-04 (L); Model SAS-001-05 (XL)) | SEC | Unknown | Active Protective Technologies, Inc. | accessdata.fda.gov |
Compare with other makers
Updated April 9, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.