SafeSiders 5031-25/06

by Essential Dental Systems

SafeSiders 5031-25/06 is a Class I device made by Essential Dental Systems, listed in FDA GUDID since 17 Jul 2020 (UDI-DI 00766054001102), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00766054001102 UDI-DI	Date17 Jul 2020Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00766054001102

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: SafeSiders
Generic name: Manual endodontic file/rasp, reusable
Model / Ref / Catalog: 5031-25/06

Primary DI / UDI-DI: 00766054001102
FDA product code: EKP
GMDN term: Manual endodontic file/rasp, reusable

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

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Prescription use
Premarket exempt
Lot / batch number

Other properties (11, all answered No)