Polygon Drill # 2

by Overfibers SRL

Polygon Drill # 2 (PYD02) is a Class I device made by Overfibers SRL, listed in FDA GUDID since 21 Feb 2025 (UDI-DI 08059388440382), registry data as of 31 May 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 31 May 2026.

Regulatory status

as of registry sync 31 May 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number08059388440382 UDI-DI	Date21 Feb 2025Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 08059388440382

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name: Rotary/reciprocating endodontic file/rasp, reusable
Model / Ref / Catalog: Polygon Drill # 2, PYD02

Primary DI / UDI-DI: 08059388440382
FDA product code: DZA
GMDN term: Rotary/reciprocating endodontic file/rasp, reusable

Device class: Class I
Regulation number: 872.4130
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
Manufacturing date

Other properties (10, all answered No)