Data / Medical devices / United States / Alien Milling Technologies

Alien Milling Technologies: FDA-registered device maker in Glendora, CA, United States, 6 510(k) clearances

Name: Alien Milling Technologies FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Alien Milling Technologies is registered with the FDA (registration 3013376795) in Glendora, CA, United States. It lists 4 device types. The FDA files 6 510(k) clearances under its listings, the newest dated January 9, 2026. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number: 3013376795
Address: 614 S. Glendora Ave., Glendora, CA, United States, 91740
Owner or operator: Alien Milling Technologies (10055155)
Roles: Contract manufacturer, Manufacturer, Repackager or relabeler
First device listed: June 13, 2017
Registered through: 2027
Brand names listed: Alien Aligners, Alien Extreme, Alien HT, Alien Multi-Layer, Alien Multi-Layer 2, Blue Sky Bio Custom Titanium Abutment, DESS Custom Titanium Abutments, DESS Dental Smart Solution and more

Devices it lists

Device	Product code	Class	Role	Source
Abutment, Implant, Dental, Endosseous	NHA	2	Contract manufacturer	accessdata.fda.gov
Aligner, Sequential	NXC	2	Manufacturer	accessdata.fda.gov
Implant, Endosseous, Root-Form	DZE	2	Contract manufacturer	accessdata.fda.gov
Powder, Porcelain	EIH	2	Repackager or relabeler	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
January 9, 2026	K253973	Gradual Dental Zirconia Blank - GT(F) P1, GT(F) P2, and SP Series	EIH	Substantially Equivalent	Liaoning Upcera Co., Ltd.	accessdata.fda.gov
July 26, 2024	K241187	Alien Aligners	NXC	Substantially Equivalent	Alien Milling Technologies	accessdata.fda.gov
September 7, 2023	K231687	Gradual Dental Zirconia Blank	EIH	Substantially Equivalent	Liaoning Upcera Co., Ltd.	accessdata.fda.gov
September 2, 2018	K181167	Upcera Glaze Paste, Glaze Powder, and Glaze Liquid	EIH	Substantially Equivalent	Liaoning Upcera Co., Ltd.	accessdata.fda.gov
December 4, 2015	K152175	Upcera Dental Zirconia Blank for Aesthetic Restoration	EIH	Substantially Equivalent	Liaoning Upcera Co., Ltd.	accessdata.fda.gov
October 22, 2014	K141724	UPCERA DENTAL ZIRCONIA BLANK & DENTAL ZIRCONIA PRE-SHADED BLANK	EIH	Substantially Equivalent	Liaoning Upcera Co., Ltd.	accessdata.fda.gov

Compare with other makers

Updated January 9, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.