# K082180: Perma Fiber,Model 441; Perma Mesh, Model 440

- Pathway: 510(k) (Traditional)
- Applicant: Angelus Industria DE Productos Odontologicos
- Decided: Dec 17, 2008 after 138 days
- Product code: EBI (Resin, Denture, Relining, Repairing, Rebasing)
- Device class: 2
- Regulation: 21 CFR 872.3760
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Indications for use
Perma Fiber / Perma Mesh is indicated for use as reinforcement for: · Manufacturing or repair of full or partial dentures, overdentures and orthodontic appliances · Temporary and/or permanent plastic/composite crowns and bridges · Custom splinting for immobilization of teeth

Source page: https://510kreport.com/device/K082180
Methodology: https://510kreport.com/methodology