Kegel SG-03

by Star Port Inc

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00860015727312 UDI-DI	Date27 Apr 2026Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Kegel
Generic Name: Scar-management dressing, reusable
Model / Reference: SG-03

Primary DI / UDI-DI: 00860015727312
FDA Product Code: PFP
GMDN Term: Scar-management dressing, reusable

Device Class: Class I
Regulation Number: 878.4025
GUDID distribution status: In Commercial Distribution

Other devices from Star Port Inc

Kegel SC-03

Class I
Kegel HD-05

Class I
Niskeederm HCD-R-03

Class I
Niskeederm HCD-L-03

Class I

Properties

Premarket Exempt
Lot / Batch Number
Expiration Date
Manufacturing Date

Other properties (10)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Prescription Use: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Serial Number: No