Data / Medical devices / United States / Anchor Products Co.
Anchor Products Co.: FDA-registered device maker in Addison, IL, United States, 2 510(k) clearances
Anchor Products Co. is registered with the FDA (registration 1416891) in Addison, IL, United States. It lists 9 device types. The FDA files 2 510(k) clearances under its listings, the newest dated September 23, 2009. 1 recall event names it as the recalling firm. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 1416891
- Address
- 52 Official RD., Addison, IL, United States, 60101
- Owner or operator
- ANCHOR PRODUCTS CO. (1416891)
- Roles
- Manufacturer
- First device listed
- November 15, 1990
- Registered through
- 2026
- Brand names listed
- Anchor Brand, COUNT-TAINER, TISSUE RETRIEVAL SYSTEM
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Container, Sharps | MMK | 2 | Manufacturer | accessdata.fda.gov |
| Instrument, Surgical, Non-Powered | HAO | 1 | Manufacturer | accessdata.fda.gov |
| Knife, Myringotomy | JYP | 1 | Manufacturer | accessdata.fda.gov |
| Knife, Ophthalmic | HNN | 1 | Manufacturer | accessdata.fda.gov |
| Laparoscope, General & Plastic Surgery | GCJ | 2 | Manufacturer | accessdata.fda.gov |
| Needle, Ophthalmic Suturing | HNM | 1 | Manufacturer | accessdata.fda.gov |
| Needle, Suturing, Disposable | GAB | 1 | Manufacturer | accessdata.fda.gov |
| Needle, Suturing, Reusable | GDL | 1 | Manufacturer | accessdata.fda.gov |
| Needle, Tonsil Suturing | KBR | 1 | Manufacturer | accessdata.fda.gov |
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 |
|---|---|---|---|---|---|---|
| September 23, 2009 | K091930 | ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM, MODEL TRS100SB | GCJ | Substantially Equivalent | Anchor Products Co. | accessdata.fda.gov |
| March 26, 1979 | K790405 | ANCHOR BRAND COUNT-TAINER | MMK | Substantially Equivalent | Anchor Products Co. | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| December 9, 2010 | 57432 | Not yet classified | Terminated | Anchor Tissue Retrieval System; ETO sterilized, single use disposable device; port size 10 mm, 225 mL capacity; 3 units per box; Manufacturer: Anchor Products Co., 52 Official Rd, Addison, IL 60101 U.S.A.; Ref TRS100SB T | 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. | accessdata.fda.gov |
Compare with other makers
- All makers of Knife, Myringotomy
- All makers of Instrument, Surgical, Non-Powered
- All makers of Laparoscope, General & Plastic Surgery
- All makers of Needle, Tonsil Suturing
- All makers of Needle, Suturing, Reusable
- All makers of Needle, Suturing, Disposable
Updated March 7, 2011. 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.