SCRIBE OPCO, LLC DBA KOOZIE GROUP

FDA Device Registration & Listing · Spring Hill, FL, US · Registration 3043840147

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3043840147
FEI Number
3043840147
Entity Name
SCRIBE OPCO, LLC DBA KOOZIE GROUP
City/State/Country
Spring Hill, FL, US
Establishment Address
14799 Shady Hills Rd, Spring Hill, FL 34610, US
Establishment Type(s)
Repack or Relabel Medical Device,Manufacture Medical Device
Owner / Operator
Scribe OpCo, LLC dba Koozie Group (Owner Number: 10095511)
Owner / Operator Contact Address
14421 Myerlake Circle, Clearwater, FL 33760, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

PILL7USA , PILL7XL FA164

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NXB Dispenser, Solid Medication Physical Medicine Class 1 890.5050 2026-03-23
OHY Pill Crusher/Cutter General Hospital Class 1 880.6430 2026-03-23
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2026-03-23

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Scribe OpCo, LLC dba Koozie Group
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K944481 Garan Scientific, Inc. THE HEART PROTECTOR 1995-04-10
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29
K870091 Avery Intl. IV SECUREMENT DEVICE USING PCCE THERMO. FILM 1987-02-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043840147. Last updated year: 2026. Please use registration number 3043840147 when referencing this establishment in official correspondence.
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