Surgical devices · 21 CFR 872 Subpart E

Periodontic Marker

FDA device type “Marker, Periodontic”.

FDA codeEMPClass121 CFR872.4565Pathway510(k) exemptCategoryDental hand instruments
Companies listing it
1714 makers
Brands and models
24
510(k) clearances
00 in five years
FDA name
Marker, Periodontic

Companies that list EMP

17 companies currently list this device type with FDA.

CompanyCountryRoleBrands and models listedClearancesLatest
Hu-Friedy Mfg Co., LLCUnited StatesMakerPeriodonitic Marker82012
Integra LifeSciences CorporationUnited StatesMakerMiltex22014
Storz AM Mark GmbHGermanyMakerPocket Marking Tweezers22008
Osung Mnd Co LtdSouth KoreaMakerOGBH018 · OGBH022 · OGPA · OGPP · +6——
Dentaurum GmbH & Co. KGGermanyMakertomas-X marker——
Aspen Surgical ProductsUnited StatesMakerSymmetry Surgical——
Cislak Manufacturing, Inc.United StatesMakerCislak · Zoll Dental——
Aesculap AGGermanyMakerPERIODONTIC MARKER——
Adolf Schweick Hardt GmbH & CoGermanyMakerPOCKET MARKER——
Dentag SRLItalyMakerDENTAG——
Nawaz and SonsPakistanMakerEMP / MARKER, PERIODONTIC——
Kohler Medizintechnik GmbHGermanyMaker———
Medic UniqueUnited StatesMakerMedic Unique——
Faulhaber Pinzetten KGGermanyMaker———
Young Innovations IncUnited StatesContract manufacturer—232025
Dentimed Sao Joao LLCUnited StatesRepacker / relabelerANGELUS——
Ortho Arch Company IncUnited StatesRepacker / relabelerArch Markers——

Official records: FDA product classification for EMP · 21 CFR 872.4565.

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