Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015547002

FEI Number

3015547002

Entity Name

SWEETBIO

City/State/Country

Memphis, TN, US

Establishment Address

460 S. Highland St., Floor 2, Memphis, TN 38111, US

Establishment Type(s)

Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

SweetBio (Owner Number: 10060718)

Owner / Operator Contact Address

20 Dudley Street, Suite 900, Memphis, TN 38103, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K222143

PMA Number

N/A

All Registered Proprietary Names

APIS VERIS

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FRO	Dressing, Wound, Drug	Unknown	Class U	N/A	2023-12-04

Official Correspondent

Kayla Graff

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SweetBio

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
K150256	Argentum Medical	SILVERLON BURN CONTACT DRESSINGS	2015-04-30

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0003-06	B. Braun Medical, Inc.	U	D-Stat Dry Hemostatic Bandage. The product is an adhesive bandage.
Z-0038-2025	3M Company Health Care Business 3m Center	U	3M Tegaderm CHG, Chlorhexidine Gluconate I.V. Securement Dressing, REF 1658R

Similar Registrations

Registration Number	Establishment Name	Location
3010067148	SERIOUSLY CLEAN LTD	Nixa, MO, US
3043618351	NEORES D.O.O.	Mursko Sredisce Medimurska Zupanija, HR
3007128716	Medline Industries, LP	Norristown, PA, US
3012456427	UFP TECHNOLOGIES, INC.	Newburyport, MA, US
3019843904	OMEZA, LLC	Sarasota, FL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015547002. Last updated year: 2026. Please use registration number 3015547002 when referencing this establishment in official correspondence.