Colmed, Ltd.
Mchenry, IL, US
Colmed, Ltd. appears in FDA device records in Mchenry, IL. FDA records list 7 510(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
- 7
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 7 510(k) clearances for Colmed, Ltd. between 1979 and 1981. The busiest year on record is 1980, with 3. The most recent is 1981, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1979 | 1 |
| 1980 | 3 |
| 1981 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K811209 | JACOB WIRZ TRANSFIXATION PIN | ELS | Substantially Equivalent | |
| K810636 | VARIODRAIN | GCY | Substantially Equivalent | |
| K810117 | HALOGEN HEADLIGHT SYSTEM | EBA | Substantially Equivalent | |
| K801208 | HOLLOW BASKET TITANIUM DENTAL IMPLANT | ELE | Substantially Equivalent | |
| K801006 | CHARNLEY DESIGN HIP PROSTHESIS | JDG | Substantially Equivalent | |
| K800762 | PS3 TITANIUM SCREW DENTAL IMPLANT | DZE | Substantially Equivalent | |
| K792241 | PELIMIT | IRN | 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