Prabadin Corp (other, Miami, FL): 23 new FDA device listings, incl. visual, pregnancy hcg, prescription use
Prabadin Corp (Miami, Florida): 23 new FDA device listings, incl. visual, pregnancy hcg, prescription use. Its amount of 23 is top-decile (97th percentile of 2,570 records). Dated 103 days ago, it serves as a historical benchmark. Score 65/100. 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: 23 · 97th percentile of 2,570 DeviceEstablishmentPulse records · 23.0x 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 | Prabadin Corp |
| Role | Other |
| Establishment types | Complaint File Establishment per 21 CFR 820.198 |
| Location | Miami, FL, US |
| New listings | 23 |
| Devices | Visual, Pregnancy Hcg, Prescription Use; Electrosurgical, Cutting & Coagulation & Accessories; Test, Cocaine And Cocaine Metabolites, Over The Counter; Test, Methamphetamine, Over The Counter; Test, Barbiturate, Over The Counter; Test, Tricyclic Antidepressants, Over The Counter; Test, Benzodiazepine, Over The Counter; Test, Cannabinoid, Over The Counter; Test, Methadone, Over The Counter; Test, Phencyclidine (Pcp), Over The Counter |
| Product codes | JHI, GEI, NFY, NGG, PTH, QAW, NFV, NFW, PTG, NGM, QBF, NGL, NFT, FZZ, GDX |
| Device classes | Class I, Class II, Unclassified |
| Medical specialties | Clinical Chemistry, General, Plastic Surgery, Clinical Toxicology, General Hospital |
| Brand names | Visual Pregnancy Test HCG; CAUTERY PUSH BUTTON; Drug Cup Test Multiple; SKIN MARKER; SCALPAL; LIGHT HANDLE COVER; NEEDLE COUNTER; Jackson Pratt Drainage Set |
| First new listing | 2026-07-08 |
| Latest new listing | 2026-07-24 |
| FDA registration number | 3016659819 |
| Registration expires | 2026-12-31 |
| amount percentile | 97th of 2,570 (median 1, 23.0x 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: 2026-07-24
- Data refreshed: 2026-10-28
- Refunds on request within 14 days
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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: Prabadin Corp and 84 Florida peers
- Florida DeviceEstablishmentPulse records like this one: 84
- Prabadin Corp's amount: 97th 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)
65 / 100 Score
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.
What is the DeviceEstablishmentPulse record for Prabadin Corp in Miami, Florida?
Prabadin Corp (Miami, FL), a other, added 23 FDA device listings between 2026-07-08 and 2026-07-24.
How does Prabadin Corp compare to other Florida DeviceEstablishmentPulse records?
This is a top-decile record: its amount of 23 is 23.0x the median of 1 across 2,570 records. It is 103 days old; check the official source for later updates before acting.
Prabadin Corp vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Prabadin Corp | Miami, FL | 23 | 97th | 2026-07-24 |
| Ortho Max Inc | Palm City, FL | 14 | 96th | 2026-08-26 |
| Advance-Esthetic LLC | Fort Lauderdale, FL | 8 | 91st | 2026-10-12 |
| Metier Medical (USA) LLC | Ponte Vedra Beach, FL | 7 | 90th | 2026-10-16 |
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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.