Eisertech, LLC
San Diego, CA, US
Eisertech, LLC appears in FDA device records in San Diego, CA. FDA records list 8 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 8
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 8 510(k) clearances for Eisertech, LLC between 2011 and 2019. The busiest year on record is 2012, with 3. The most recent is 2019, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2011 | 1 |
| 2012 | 3 |
| 2015 | 2 |
| 2019 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K192768 | Temporary Fixation Pins | JDW | Substantially Equivalent | |
| K190565 | Cervical Plate | KWQ | Substantially Equivalent | |
| K140348 | INTERBODY CAGE | MAX | Substantially Equivalent | |
| K142576 | Spinal System | NKB | Substantially Equivalent | |
| K122444 | CERVICAL CAGE | ODP | Substantially Equivalent | |
| K113170 | CERVICAL PLATE | KWQ | Substantially Equivalent | |
| K113478 | PLIF CAGE | MAX | Substantially Equivalent | |
| K110915 | CERVICAL CAGE | ODP | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain