FDA Device Establishments · JSON-LD · Markdown
FEI 3005061536 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3005061536 |
|---|---|
| Owner / Operator | Tecomet (#1828464) |
| Address | 111 N. CLAY, CLAYPOOL, IN, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | JDW, KTT |
| Regulation § (21 CFR) | 888.3040, 888.3030 |
| Proprietary names | Ace Fisher External Fixation Device; ACE FISCHER EXTERNAL FIXATION SYSTEM/ACE-FISCHER(R), TEMPFIX(R), HOFFMAN CLASSIC(TM) EXTERNAL FIXATORS; ACE FISCHER EXTERNAL FIXATION SYSTEM/ACE FISCHER EXTERNAL FIXATION DEVICE/ACE-FISCHER(R), TEMPFIX(R), HOFFMAN CLASSIC(TM) EXTERNAL FIXATORS; FOOT FRAME CROSS BAR; Appliance, fixation, nail/blade/plate combination, multiple component; Ace External Fixation |
Source: openFDA. Public-domain (CC0).