# Anclote Manufacturing Company (contract manufacturer, Largo, FL): 1 new FDA device listing, incl. prosthesis, thigh socket, external component

**Score:** 50/100

| Field | Value |
|---|---|
| Establishment | Anclote Manufacturing Company |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device; Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Largo, FL, US |
| New listings | 1 |
| Devices | Prosthesis, Thigh Socket, External Component |
| Product codes | ISS |
| Device classes | Class I |
| Medical specialties | Physical Medicine |
| Brand names | AK Auto Expulsion Valve (VAER); Anclote Elevated Vacuum Pump (AEVP); Anclote Suction Plate (PSSP,PSTH); FlexForm (FISP) Flexible Inner Socket; Anclote Vented Distal Cusions (DCSP) |
| First new listing | 2026-06-02 |
| Latest new listing | 2026-06-02 |
| FDA registration number | 3045526569 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- U.S. establishment.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-11-04T21:52:36.524Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.