Anclote Manufacturing Company (contract manufacturer, Largo, FL): 1 new FDA device listing, incl. prosthesis, thigh socket, external component
Anclote Manufacturing Company (Largo, Florida): 1 new FDA device listing, incl. prosthesis, thigh socket, external component. Its amount of 1 is above the median of 1 (50th percentile). Dated 155 days ago, it serves as a historical benchmark. Score 50/100. As of 2026-10-28, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).
Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
amount: 1 · 50th percentile of 2,570 DeviceEstablishmentPulse records · 1.0x the median
Free preview: all 14 published fields of this record are shown below. Locked: 83 related FL DeviceEstablishmentPulse records and the 5-column CSV export.
| 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 | Anclote Vented Distal Cusions (DCSP); Anclote Suction Plate (PSSP,PSTH); FlexForm (FISP) Flexible Inner Socket; AK Auto Expulsion Valve (VAER); Anclote Elevated Vacuum Pump (AEVP) |
| First new listing | 2026-06-02 |
| Latest new listing | 2026-06-02 |
| FDA registration number | 3045526569 |
| Registration expires | 2026-12-31 |
| amount percentile | 50th of 2,570 (median 1, 1.0x median) |
| Peer records CSV (84 FL records) | 🔒 Click to unlock → |
| CRM-ready export with official source URLs | 🔒 Click to unlock → |
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL
- Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
- Record date: 2026-06-02
- Data refreshed: 2026-10-28
- Refunds on request within 14 days
Top DeviceEstablishmentPulse records (FL first): Oketz Logistics LLC (repackager or relabeler, Coral Gables, · Zapalign LLC (repackager or relabeler, Fort Lauderdale, FL) · Stellmacher Instruments Inc (repackager or relabeler, Orland · Surgipros LLC (repackager or relabeler, Palmetto, FL) · Structure Medical, LLC. (contract manufacturer, Naples, FL) · Browse all by state and category →
LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 28 Oct 2026 20:51:27 GMT
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Peer benchmark and outreach value: Anclote Manufacturing Company and 84 Florida peers
- Florida DeviceEstablishmentPulse records like this one: 84
- Anclote Manufacturing Company's amount: 50th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Florida peer: $16,800 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
50 / 100 Score
- Contract manufacturer or sterilizer adding work.
- U.S. establishment.
What is the DeviceEstablishmentPulse record for Anclote Manufacturing Company in Largo, Florida?
Anclote Manufacturing Company (Largo, FL), a contract manufacturer, added 1 FDA device listing on 2026-06-02.
How does Anclote Manufacturing Company compare to other Florida DeviceEstablishmentPulse records?
Its amount of 1 sits in the upper half (50th percentile) of 2,570 records; the median is 1. It is 155 days old; check the official source for later updates before acting.
Anclote Manufacturing Company vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Anclote Manufacturing Company | Largo, FL | 1 | 50th | 2026-06-02 |
| Tecomet Inc. | Wilmington, MA | 3 | 77th | 2026-10-15 |
| Bard Shannon Limited | Humacao, PR | 3 | 77th | 2026-10-14 |
| Orchid Orthopedic Solutions Oregon, Inc. | Oregon City, OR | 3 | 77th | 2026-10-05 |
Related records
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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.