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Sign in to claim this brandANCHOR PRODUCTS CO.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 52 OFFICIAL RD., ADDISON, IL, 60101
- Website
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- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 1416891
- DUNS Number
- —
Catalogue (22)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tissue Retrieval System | TRS175SB2 | FDA UDI | Class II | Active |
| Tissue Retrieval System | TRS100SB2 | FDA UDI | Class II | Active |
| Tissue Retrieval System | TRS-TV-25 | FDA UDI | Class II | Active |
| Count-Tainer 40 | 5100F | FDA UDI | Class II | Active |
| Tissue Retrieval System | TRS090 | FDA UDI | Class II | Active |
| Tissue Retrieval System | TRS-ROBO-8 | FDA UDI | Class II | Active |
| Tissue Retrieval System | TRS080 | FDA UDI | Class II | Active |
| Count-Tainer 20 | 5120FNS | FDA UDI | Class II | Active |
| Count-Tainer 20 | 5120F | FDA UDI | Class II | Active |
| Tissue Retrieval System | TRS-VATS-15 | FDA UDI | Class II | Active |
| Tissue Retrieval System | TRS210 | FDA UDI | Class II | Active |
| Tissue Retrieval System | TRS-ROBO-12 | FDA UDI | Class II | Active |
| Count-Tainer 40 | 5100FNS | FDA UDI | Class II | Active |
| Tissue Retrieval System | TRS190SB2 | FDA UDI | Class II | Active |
| Tissue Retrieval System | TRS070 | FDA UDI | Class II | Active |
| Anchor Biopsy Needle | K873124 | FDA 510(k) | Class I | Active |
| Anchor Laparoscopic Tissue Retrieval System, Model Trs100sb | K091930 | FDA 510(k) | Class II | Active |
| Anchor Double-Edge Myringotomy Blade | K884862 | FDA 510(k) | Class I | Active |
| Anchor Laparoscopic Tissue Retrieval System | K982073 | FDA 510(k) | Class II | Active |
| Anchor Brand Count-Tainer | K790405 | FDA 510(k) | Class II | Active |
| Anchor Laparscopic Tissue Retieval System | K061555 | FDA 510(k) | Class II | Active |
| Anchor Brand Surgical Needles | K831648 | FDA 510(k) | Class I | Active |
Related Companies
Authorised Representatives
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FDA Recalls (2)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Dec 9, 2010 | Z-1591-2011 | — | terminated | The metal component within the unit can break and cause a malfunction. Use of the device may represent a potential health hazard if the metal component is not removed after breakage. |
| Dec 9, 2010 | Z-1590-2011 | — | terminated | The metal component within the unit can break and cause a malfunction. Use of the device may represent a potential health hazard if the metal component is not removed after breakage. |