Plasdent 8015-HJ

by Plasdent Corp.

Plasdent 8015-HJ is a Class I device made by Plasdent Corp., listed in FDA GUDID since 6 Jan 2022 (UDI-DI D8328015HJ1), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberD8328015HJ1 UDI-DI	Date6 Jan 2022Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Plasdent
Generic name: Dental suction system cannula, single-use
Model / Ref / Catalog: 8015-HJ

Primary DI / UDI-DI: D8328015HJ1
FDA product code: EHZ
GMDN term: Dental suction system cannula, single-use

Device class: Class I
Regulation number: 872.6640
GUDID distribution status: In Commercial Distribution

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Properties

Single use
Premarket exempt

Other properties (13, all answered No)