Manufacturer registered with FDA

Tech West Inc.

Fresno, CA, United States. Lists 1 dental device type with FDA across 1 registered establishment.

FDA owner/operator10028887Manufacturer
Device types listed
1
Brands and models
51
510(k) clearances
0as applicant
Markets registered in
22 registrations outside the US
Establishments
1United States

Registered in 2 markets

Where regulators' registries name Tech West Inc. as the manufacturer or the registration holder of a device.

All markets
United States: 1 device types listedTaiwan: 2 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerTech West Inc.1 device types—Below
TaiwanTFDAManufacturerTECH WEST INC.22009–2020Pure 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 Tech West Inc. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Accessories Operative Dental UnitNRD · Class 1—Maker
ACL10S2ACL10S5ACL15S5ACL20D5ACL30D5ACL40D5ACL60D5ACL80D5ACO4D2ACO6T2
41 more
ACOR2D1ACOR2D1QACOR2D2ACOR2D2QEcoVac Vacuum Pumps:Oilless Series Elite Air Compressors:Oilless Series Rocky Air Compressors:Product NameVPD10D2VPD10S2VPD120D5VPD20D5VPD20S5VPD2S2VPD30D5VPD40D5VPD4D2VPD5S2VPD60D5VPD80D5VPL12T2VPL12T2RVPL2SSVPL2SSRVPL3SSVPL3SSRVPL4D2VPL4D2RVPL4S2VPL4S2RVPL6D2VPL6D2RVPL8D2VPL8D2RVPL9T2VPL9T2RVPLG3SSVPLG3SSRVPLG5SSVPLG5SSRWhirlWind GoldenVac Vacuum Pumps:
2023

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
TECH WEST INC.FDA reg. 3003172176Fresno, CA, United StatesManufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10028887). 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.