Skip to content

FlexiNylon Natural 1kg

by Perflex

FlexiNylon Natural 1kg (22005) is a Class II device made by Perflex, listed in FDA GUDID since 15 Jun 2020 (UDI-DI 07290110500450), 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

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07290110500450 UDI-DI Date15 Jun 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
FlexiNylon
Generic name
Dental appliance fabrication material, thermoplastic
Model / Ref / Catalog
Natural 1kg, 22005
Primary DI / UDI-DI
07290110500450
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

Related devices

Category: Dental appliance fabrication material, thermoplastic

Other devices from Perflex

See all devices from Perflex →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)