Data / Medical devices / United States / Micro Medical Devices, Inc.

Micro Medical Devices, Inc.: FDA-registered device maker in Calabasas, CA, United States, 1 510(k) clearance

Name: Micro Medical Devices, Inc. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Micro Medical Devices, Inc. is registered with the FDA (registration 3004574050) in Calabasas, CA, United States. It lists 11 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 10, 2004. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers like this one Watch Micro Medical Devices, Inc.

FDA registration number: 3004574050
Address: 23945 Calabasas RD. Suite 110, Calabasas, CA, United States, 91302
Owner or operator: MICRO MEDICAL DEVICES, INC. (9061275)
Roles: Complaint file establishment, Manufacturer, Manufacturer for export
First device listed: November 20, 2007
Registered through: 2026
Brand names listed: OMNI CXL, PalmScan DA 2000, PalmScan K2000, PalmScan PM2000, PalmScan STB 2000, PalmScan VF2000, PalmScan VS2000, Palmscan AP2000, A2000, P2000, P2000Fp

Devices it lists

Device	Product code	Class	Role	Source
Adaptometer (Biophotometer), Software-Based Data Acquisition And Stimulus Generation	OUM	1	Complaint file establishment, Manufacturer	accessdata.fda.gov
Digital Visual Acuity Test	QTO	1	Complaint file establishment, Manufacturer	accessdata.fda.gov
Haploscope	HJT	1	Manufacturer	accessdata.fda.gov
Instrument, Measuring, Stereopsis	HLC	1	Complaint file establishment, Manufacturer	accessdata.fda.gov
Lamp, Uvc, (For Treating Skin And Wounds)	MXG	2	Manufacturer for export	accessdata.fda.gov
Perimeter, Automatic, Ac-Powered	HPT	1	Complaint file establishment, Manufacturer	accessdata.fda.gov
Pupillograph	HRI	1	Complaint file establishment, Manufacturer	accessdata.fda.gov
System, Imaging, Pulsed Echo, Ultrasonic	IYO	2	Complaint file establishment, Manufacturer	accessdata.fda.gov
Tester, Color Vision	HIT	1	Complaint file establishment, Manufacturer	accessdata.fda.gov
Topographer, Corneal, Battery Powered	NOG	1	Complaint file establishment, Manufacturer	accessdata.fda.gov
Transducer, Ultrasonic, Diagnostic	ITX	2	Complaint file establishment, Manufacturer	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
December 10, 2004	K043287	PALMSCAN AP2000; PALMSCAN A2000; PALMSCAN P2000	IYO	Substantially Equivalent	Micromedical Devices, Inc.	accessdata.fda.gov

Compare with other makers

Updated December 10, 2004. 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.