Gfa Production Inc (specification developer, Clearwater, FL): 25 new FDA device listings, incl. finger cot

Gfa Production Inc (Clearwater, Florida): 25 new FDA device listings, incl. finger cot. Its amount of 25 is top-decile (98th percentile of 2,570 records). Dated 96 days ago, it serves as a historical benchmark. Score 70/100. 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: 25 · 98th percentile of 2,570 DeviceEstablishmentPulse records · 25.0x the median

Free preview: all 15 published fields of this record are shown below. Locked: 83 related FL DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentGfa Production Inc
Owner / operatorGFA Production Inc
RoleSpecification developer (outsources manufacturing)
Establishment typesDevelop Specifications But Do Not Manufacture At This Facility; Repack or Relabel Medical Device
LocationClearwater, FL, US
New listings25
DevicesFinger Cot; Protector, Skin Pressure; Forceps; Dressing, Wound, Hydrogel Without Drug And/Or Biologic; Stapler, Skin; Pack, Hot Or Cold, Disposable; Brush, Scrub, Operating-Room; Bedding, Disposable, Medical; Gauze / Sponge,Nonresorbable For External Use; Bandage, Cast
Product codesLZB, FMP, HTD, NAE, QQS, IMD, GEC, KME, NAB, ITG, KGX, OHO, NOC, KXG, FQZ
Device classesClass I, Not classified
Medical specialtiesGeneral Hospital, General, Plastic Surgery, Physical Medicine, Anesthesiology, Ophthalmic
Brand namesFinger Cot; Face Shield; Tweezers/Forceps; Burn dressing, Burn gel dressing; Disposable Skin Stapler; Instant Cold Compress; Moleskin; Emergency Blanket
First new listing2026-06-12
Latest new listing2026-07-31
FDA registration number3045526618
Registration expires2026-12-31
amount percentile98th of 2,570 (median 1, 25.0x median)
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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: 2026-07-31
  • 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: Gfa Production Inc and 84 Florida peers

  • Florida DeviceEstablishmentPulse records like this one: 84
  • Gfa Production Inc's amount: 98th 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)

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70 / 100 Score

  • Brings its own devices to market: buys manufacturing, sterilization and QMS help.
  • Several new listings at once.
  • U.S. establishment.

What is the DeviceEstablishmentPulse record for Gfa Production Inc in Clearwater, Florida?

Gfa Production Inc (Clearwater, FL), a specification developer (outsources manufacturing), added 25 FDA device listings between 2026-06-12 and 2026-07-31.

How does Gfa Production Inc compare to other Florida DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 25 is 25.0x the median of 1 across 2,570 records. It is 96 days old; check the official source for later updates before acting. Its Score of 70/100 puts it among the stronger signals in this feed.

Gfa Production Inc vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Gfa Production IncClearwater, FL2598th2026-07-31
Arthrex, Inc.Naples, FL1295th2026-09-27
Boston Scientific CorporationMarlborough, MA992nd2026-10-16
Sol-Millennium Medical, Inc.Chicago, IL891st2026-09-28

Related records

DeviceEstablishmentPulse: Specification developer (outsources manufacturing) DeviceEstablishmentPulse: U.S. establishment DeviceEstablishmentPulse: records in Florida

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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.

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