WELLY HEALTH PBC

FDA Device Registration & Listing · Minneapolis, MN, US · Registration 3016050930

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
3016050930
FEI Number
3016050930
Entity Name
WELLY HEALTH PBC
City/State/Country
Minneapolis, MN, US
Establishment Address
700 Nicollet Mall, Suite 800, Minneapolis, MN 55402, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Welly Health PBC (Owner Number: 10061905)
Owner / Operator Contact Address
700 Nicollet Mall, Suite 800, Minneapolis, MN 55402, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ILH Splint, Hand, And Components Physical Medicine Class 1 890.3475 2026-03-25
HTD Forceps General, Plastic Surgery Class 1 878.4800 2026-03-25
KXF Applicator, Absorbent Tipped, Non-Sterile General Hospital Class 1 880.6025 2026-03-25
LRR First Aid Kit With Drug Unknown Class N N/A 2019-12-02
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2019-12-02
OHO First Aid Kit Without Drug General, Plastic Surgery Class 1 878.4014 2019-12-02
NAC Dressing, Wound, Hydrophilic General, Plastic Surgery Class 1 878.4018 2019-12-02
JOK Scissors, Medical, Disposable General Hospital Class 1 880.6820 2026-03-25
FQM Bandage, Elastic General Hospital Class 1 880.5075 2026-03-25
LYA Splint, Intranasal Septal Ear, Nose, Throat Class 1 874.4780 2026-03-25

Official Correspondent

Joseph Ciccone

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Welly Health PBC
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
K852723 The Huxley Instrument Corp. FOERSTER SPONGE FORCEPS, SERRATED, 7+SS 410 OR 420 1985-07-15
K873512 Arthropedics, Inc. SERRATED GRASPING FORCEPS, RIGHT 1987-11-02
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

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3041725026 Fill Mill Lakewood, NJ, US
3012316249 COMPASS HEALTH BRANDS (CORPORATE OFFICE) Middleburg Heights, OH, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016050930. Last updated year: 2026. Please use registration number 3016050930 when referencing this establishment in official correspondence.
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