Data / Medical devices / United States / Medical Technical Products, Inc
Medical Technical Products, Inc: FDA-registered device maker in Irvine, CA, United States, 3 510(k) clearances
Medical Technical Products, Inc is registered with the FDA (registration 2025303) in Irvine, CA, United States. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated September 22, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2025303
- Address
- 9251 Irvine Boulevard, Irvine, CA, United States, 92618
- Owner or operator
- Medical Technical Products, Inc (2025303)
- Roles
- Manufacturer
- First device listed
- December 12, 2007
- Registered through
- 2026
- Brand names listed
- LightSonic Phacoemulsification System, Model 2000 Ophthalmic Surgical Sys, Model 3000 Phacoemulsification System, Trisonic Phacoemulsification System, US Handpiece, US Handpiece, Mini
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Needle, Phacoemulsification, Reprocessed | NKX | 2 | Manufacturer | accessdata.fda.gov |
| Unit, Phacofragmentation | HQC | 2 | 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 |
|---|---|---|---|---|---|---|
| September 22, 2008 | K080803 | VISUAL PHACOEMULSIFICATION SYSTEM, MODEL 551 | HQC | Substantially Equivalent | American Optisurgical, Inc. | accessdata.fda.gov |
| August 4, 1994 | K940088 | MEDICAL TECHNICAL PRODUCTS STANDARD ULTRASONIC HANDPIECE | HQC | Substantially Equivalent | Medical Technical Products | accessdata.fda.gov |
| June 17, 1994 | K940084 | MODEL 2000 OPHTHALMIC SURGICAL SYSTEM | HQC | Substantially Equivalent | Medical Technical Products | accessdata.fda.gov |
Compare with other makers
Updated September 22, 2008. 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.