Centrix Endo Kit 360053

by Centrix, 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	Number00817051021218 UDI-DI	Date23 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Centrix Endo Kit
Generic name: Calcium hydroxide dental suspension
Model / reference: 360053

Primary DI / UDI-DI: 00817051021218
FDA product code: EMA, EJK
GMDN term: Calcium hydroxide dental suspension

Device class: Class II
Regulation number: 872.3275, 872.3250
GUDID distribution status: In Commercial Distribution

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Properties

Prescription use
Convenience kit
Lot / batch number
Expiration date
Manufacturing date

Other properties (10)

Supplied sterile: No
Sterilise before use: No
Single use: No
Implantable: No
Contains latex: No
Over-the-counter: No
Combination product: No
HCT/P: No
Premarket exempt: No
Serial number: No