Prosthetic devices · 21 CFR 872 Subpart D

Wire Clasp

FDA device type “Clasp, Wire”.

FDA codeEJWClass121 CFR872.3285Pathway510(k) exempt
Companies listing it
103 makers
Brands and models
9
510(k) clearances
30 in five years
FDA name
Clasp, Wire
1987: 11988: 11990: 119801990200020102020

510(k) clearances per year, 1976–2026

Companies that list EJW

10 companies currently list this device type with FDA.

CompanyCountryRoleBrands and models listedClearancesLatest
Dentaurum GmbH & Co. KGGermanyMakerClasp wire——
Falcon Surgical Co. (Pvt.) Ltd.PakistanMakerCLASP, WIRE——
Fseven Dental Technology Zhuhai Co.,ltdChinaMakerCLASP,WIRE——
CreoDent Prosthetics LTDUnited StatesRepacker / relabelerClasp92022
Keystone IndustriesUnited StatesContract manufacturerKeystone Industries Clasp Wire22025
Dentimed Sao Joao LLCUnited StatesRepacker / relabelerAngelus——
Aspen Surgical ProductsUnited StatesContract manufacturerSymmetry Surgical——
Shaw Dental Laboratories Corp.United StatesRepacker / relabelerWire Clasp——
DigiSmiles LabUnited StatesRepacker / relabelerClasp Wire——
Mainline Medical Dental SupplyCanadaForeign exporter———

510(k) clearances

Decided510(k)DeviceApplicant
25 Apr 1990K901257WIRONTOM CLASP WIREIvoclar North America, Inc.
21 Apr 1988K881331ORTHODONTIC NITINOL SPRINGSFlexmedics
21 Jul 1987K872746VITALLIUM WIREAustenal Dental, Inc.

Official records: FDA product classification for EJW · 21 CFR 872.3285.

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026