Manufacturer registered with FDA

Strauss & Co.

Ra'anana, Israel. Lists 4 dental device types with FDA across 1 registered establishment.

FDA owner/operator9011145ManufacturerPrivate-label distributor
Device types listed
4
Brands and models
2
510(k) clearances
0as applicant
Markets registered in
513 registrations outside the US
Establishments
1Israel

Registered in 5 markets

Where regulators' registries name Strauss & Co. as the manufacturer or the registration holder of a device.

All markets
United States: 4 device types listedBrazil: 5 registrationsSouth Korea: 4 registrationsIsrael: 3 registrationsTaiwan: 1 registrations
RegisteredHome: IsraelOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerStrauss & Co.4 device types—Below
BrazilANVISAManufacturerSTRAUSS & CO. COMPANY52019–2019Pure Global AI
South KoreaMFDSManufacturerSTRAUSS & COStrauss & Co.42012–2026Pure Global AI
IsraelAMARRegistration holderSTRAUSS & CO.3—Pure Global AI
TaiwanTFDAManufacturerSTRAUSS & CO.12009–2009Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

Devices listed with FDA

What Strauss & Co. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Dental Diamond InstrumentDZP · Class 1Dental burs & diamondsMaker—2009
Abrasive PointEHL · Class 1Polishing & prophylaxisLister
Strauss & Co. Polishers
2026
Dental BurEJL · Class 1Dental burs & diamondsMaker
Strauss & Co. Burs
2026
Oral Cavity Abrasive Polishing AgentEJR · Class 1Polishing & prophylaxisLister—2020

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

Registered establishments

EstablishmentLocationWhat it does
Strauss & Co.FDA reg. 3001616037Raanana Central, IsraelManufacturer, Private-label distributor

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9011145). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.