Medi-Dose, Inc. (specification developer, Warminster, PA): 1 new FDA device listing, incl. dispenser, liquid medication
Medi-Dose, Inc. (Warminster, Pennsylvania): 1 new FDA device listing, incl. dispenser, liquid medication. Its amount of 1 is above the median of 2 (50th percentile). Dated 28 days ago, it is in the active follow-up window. Score 65/100. As of 2026-11-04, 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 2,709 DeviceEstablishmentPulse records · 0.5x the median
Free preview: all 14 published fields of this record are shown below. Locked: 46 related PA DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Medi-Dose, Inc. |
| Role | Specification developer (outsources manufacturing) |
| Establishment types | Complaint File Establishment per 21 CFR 820.198; Repack or Relabel Medical Device; Develop Specifications But Do Not Manufacture At This Facility |
| Location | Warminster, PA, US |
| New listings | 1 |
| Devices | Dispenser, Liquid Medication |
| Product codes | KYX |
| Device classes | Class I |
| Medical specialties | General Hospital |
| Brand names | STERI-DROPPER |
| First new listing | 2026-10-08 |
| Latest new listing | 2026-10-08 |
| FDA registration number | 2521373 |
| Registration expires | 2027-12-31 |
| amount percentile | 50th of 2,709 (median 2, 0.5x median) |
| Peer records CSV (47 PA 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: 2026-10-08
- Data refreshed: 2026-11-04
- Refunds on request within 14 days
Top DeviceEstablishmentPulse records (PA first): Philips Ultrasound LLC (contract manufacturer, Reedsville, P · Arch Medical Solutions - Philadelphia, LLC Dba Jade Precisio · Globus Medical, Inc. (manufacturer, Audubon, PA) · Alta Smiles, LLC (manufacturer, Fort Washington, PA) · Synthes (USA) Products LLC (specification developer, West Ch · 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, 04 Nov 2026 21:52:36 GMT
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Peer benchmark and outreach value: Medi-Dose, Inc. and 47 Pennsylvania peers
- Pennsylvania DeviceEstablishmentPulse records like this one: 47
- Medi-Dose, Inc.'s amount: 50th percentile of 2,709 records
- Timing: Medium: dated in the last 30 days
- Estimated pipeline if you contact every Pennsylvania peer: $9,400 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
65 / 100 Score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- U.S. establishment.
- Listed in the last 45 days.
What is the DeviceEstablishmentPulse record for Medi-Dose, Inc. in Warminster, Pennsylvania?
Medi-Dose, Inc. (Warminster, PA), a specification developer (outsources manufacturing), added 1 FDA device listing on 2026-10-08.
How does Medi-Dose, Inc. compare to other Pennsylvania DeviceEstablishmentPulse records?
Its amount of 1 sits in the upper half (50th percentile) of 2,709 records; the median is 2. It is 28 days old, still within a typical 45-day follow-up window.
Medi-Dose, Inc. vs. top 2 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Medi-Dose, Inc. | Warminster, PA | 1 | 50th | 2026-10-08 |
| Centinel Spine, LLC | West Chester, PA | 3 | 77th | 2026-10-22 |
| Synthes (USA) Products LLC | West Chester, PA | 7 | 90th | 2026-10-23 |
Related records
DeviceEstablishmentPulse: Specification developer (outsources manufacturing) DeviceEstablishmentPulse: U.S. establishment DeviceEstablishmentPulse: records in Pennsylvania
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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.