Data / Medical devices / United States / Aei Technologies Inc.
Aei Technologies Inc.: FDA-registered device maker in Bastrop, TX, United States, 4 510(k) clearances
Aei Technologies Inc. is registered with the FDA (registration 3004055954) in Bastrop, TX, United States. It lists 3 device types. The FDA files 4 510(k) clearances under its listings, the newest dated November 1, 1996. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004055954
- Address
- 410 Technology Drive, Bastrop, TX, United States, 78602
- Owner or operator
- AEI TECHNOLOGIES INC. (9054194)
- Roles
- Manufacturer
- First device listed
- November 12, 2007
- Registered through
- 2026
- Brand names listed
- CD-3A, MAX-II, MAX-IIa, MOXUS, S-3A, S-3A/I
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase | CCK | 2 | Manufacturer | accessdata.fda.gov |
| Analyzer, Gas, Oxygen, Gaseous-Phase | CCL | 2 | Manufacturer | accessdata.fda.gov |
| Computer, Oxygen-Uptake | BZL | 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 |
|---|---|---|---|---|---|---|
| November 1, 1996 | K943824 | GASEOUS OXYGEN ANALYZER (MODEL S-3A) MODIFICATION | CCL | Substantially Equivalent | Ametek, Inc. | accessdata.fda.gov |
| February 16, 1995 | K942113 | CARBON DIOXIDE ANALYZER (MODEL CD-3A) | CCK | Substantially Equivalent | Ametek, Inc. | accessdata.fda.gov |
| April 8, 1993 | K922660 | PHYSIO-DYNE EASI - LAB | BZL | Substantially Equivalent | Physio-Dyne | accessdata.fda.gov |
| May 31, 1988 | K874663 | MOXUS OR OCM-1 OXYGEN UPTAKE SYSTEM | BZL | Substantially Equivalent | Ametek/Thermox Instruments Division | accessdata.fda.gov |
Compare with other makers
- All makers of Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
- All makers of Computer, Oxygen-Uptake
- All makers of Analyzer, Gas, Oxygen, Gaseous-Phase
Updated November 1, 1996. 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.