Data / Medical devices / United States / JMG Machine, Inc.
JMG Machine, Inc.: FDA-registered device maker in La Mirada, CA, United States, 9 510(k) clearances
JMG Machine, Inc. is registered with the FDA (registration 2031910) in La Mirada, CA, United States. It lists 16 device types. The FDA files 9 510(k) clearances under its listings, the newest dated June 6, 2012. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 2031910
- FEI number
- 3002926812
- Address
- 17037 Industry Place, La Mirada, CA, United States, 90638
- Owner or operator
- JMG MACHINE, INC. (9039528)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- January 31, 2013
- Registered through
- 2027
- Brand names listed
- Biomet, DePuy Inc, Depuy Inc, Johnson & Johnson, Light Slotted Mallet (DePuy), Symmetry Medical, Zimmer Biomet
Devices it lists
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 6, 2012 | K121064 | MAKOPLASTY TOTAL HIP APPLICATION, RIO STANDARD SYSTEM | OLO | Substantially Equivalent | Mako Surgical Corporation | accessdata.fda.gov |
| April 16, 2012 | K120291 | OP SPINE SYSTEM | OSH | Unknown | OrthoPediatrics Corp. | accessdata.fda.gov |
| March 1, 2012 | K112507 | RESTORIS PARTIAL KNEE APPLICATION (PKA), RIO STANDARD SYSTEM | OLO | Substantially Equivalent | Mako Surgical Corporation | accessdata.fda.gov |
| December 15, 2011 | K112218 | ACE-FISCHER(R), TEMPFIX(R), HOFFMAN CLASSIC(TM) EXTERNAL FIXATORS | KTT | Substantially Equivalent | DePuy Orthopaedics, Inc. | accessdata.fda.gov |
| March 23, 2009 | K083789 | ACE FISCHER EXTERNAL FIXATION SYSTEM | KTT | Substantially Equivalent | DePuy Orthopaedics, Inc. | accessdata.fda.gov |
| January 21, 2005 | K043113 | TEMPFIX EXTERNAL FIXATION SYSTEM, MR SAFE | KTT | Substantially Equivalent | DePuy Orthopaedics, Inc. | accessdata.fda.gov |
| August 26, 2002 | K021933 | TEMPFIX EXTERNAL FIXATION SYSTEM | KTT | Substantially Equivalent | DePuy Orthopaedics, Inc. | accessdata.fda.gov |
| February 22, 1994 | K936045 | ACE UNILATERAL FIXATOR II | JEC | Substantially Equivalent | Ace Orthopedic Manufacturing Co. | accessdata.fda.gov |
| September 9, 1980 | K801594 | ACE FISCHER EXTERNAL FIXATION DEVICE | HXK | Substantially Equivalent | Ace Orthopedic Manufacturing Co. | accessdata.fda.gov |
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Updated June 6, 2012. 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.