FlexNylon Light Red 200gr

FlexNylon Light Red 200gr (22010) is a Class II device made by Perflex, listed in FDA GUDID since 18 Jun 2020 (UDI-DI 07290110506421), 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	Number07290110506421 UDI-DI	Date18 Jun 2020Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 07290110506421

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: FlexNylon
Generic name: Dental appliance fabrication material, thermoplastic
Model / Ref / Catalog: Light Red 200gr, 22010
Description: FlexiNylon Thermoplastic pellets for Dentures by injection moulding Shade Light Red 200gr jar

Primary DI / UDI-DI: 07290110506421
FDA product code: EBI
GMDN term: Dental appliance fabrication material, thermoplastic

Device class: Class II
Regulation number: 872.3760
GUDID distribution status: In Commercial Distribution

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Properties

Single use
Premarket exempt
Lot / batch number
Expiration date

Other properties (11, all answered No)