Data / Medical devices / United States / Replacement Parts Industries, Inc.
Replacement Parts Industries, Inc.: FDA-registered device maker in Simi Valley, CA, United States, 3 510(k) clearances
Replacement Parts Industries, Inc. is registered with the FDA (registration 1000617661) in Simi Valley, CA, United States. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated June 13, 2002. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1000617661
- Address
- 625 Cochran St., Simi Valley, CA, United States, 93065
- Owner or operator
- Replacement Parts Industries, Inc. (10025749)
- Roles
- Repackager or relabeler, Specification developer
- First device listed
- May 6, 2008
- Registered through
- 2026
- Brand names listed
- Infant Heating Element, Infant Skin Temperature Probe, Phototherapy lamp
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Unit, Neonatal Phototherapy | LBI | 2 | Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Warmer, Infant Radiant | FMT | 2 | Repackager or relabeler, Specification developer | 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 |
|---|---|---|---|---|---|---|
| June 13, 2002 | K020966 | RPI REPLACEMENT HEATING ELEMENTS | FMT | Substantially Equivalent | Replacement Parts Industries, Inc. | accessdata.fda.gov |
| May 31, 2002 | K021531 | RPI REPLACEMENT PHOTOTHERAPY LIGHTS | LBI | Substantially Equivalent | Replacement Parts Industries, Inc. | accessdata.fda.gov |
| April 12, 2002 | K020219 | RPI SKIN OR AIR TEMPERATURE PROBE | FMT | Substantially Equivalent | Replacement Parts Industries, Inc. | accessdata.fda.gov |
Compare with other makers
Updated June 13, 2002. 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.