Well-Prep WE103-KB00

by Vericom Co., Ltd.

Well-Prep WE103-KB00 is a Class I device made by Vericom Co., Ltd., listed in FDA GUDID since 1 Nov 2016 (UDI-DI 08809254452229), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number08809254452229 UDI-DI	Date1 Nov 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 08809254452229

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Well-Prep
Generic name: Dental tooth-cleaning solution
Model / reference: WE103-KB00

Primary DI / UDI-DI: 08809254452229
FDA product code: EKQ
GMDN term: Dental tooth-cleaning solution

Device class: Class I
Regulation number: 872.4565
GUDID distribution status: In Commercial Distribution

Similar devices

Other devices filed under FDA product code EKQ (Preparer, Root Canal Endodontic).

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Properties

Prescription use
Premarket exempt
Lot / batch number
Expiration date
Manufacturing date

Other properties (10, all answered No)