Anchor Products Co.: FDA filings under this applicant name
FDA lists 7 510(k) clearances under the applicant name “Anchor Products Co.” (first 1979, latest 2009), across 5 product codes in 2 review panels. Median 510(k) review time under this name: 85 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| GCJ | Laparoscope, General & Plastic Surgery | 3 | 3 |
| GAA | Needle, Aspiration And Injection, Disposable | 1 | 1 |
| GAB | Needle, Suturing, Disposable | 1 | 1 |
| GES | Blade, Scalpel | 1 | 1 |
| MMK | Container, Sharps | 1 | 1 |
Review panels
Most recent Anchor Products Co. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K091930 | ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM, MODEL TRS100SB | GCJ | 2009-09-23 | 85 |
| K061555 | ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM | GCJ | 2006-08-31 | 87 |
| K982073 | ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM | GCJ | 1998-09-22 | 102 |
| K884862 | ANCHOR DOUBLE-EDGE MYRINGOTOMY BLADE | GES | 1988-12-27 | 36 |
| K873124 | ANCHOR BIOPSY NEEDLE | GAA | 1987-09-08 | 29 |
| K831648 | ANCHOR BRAND SURGICAL NEEDLES | GAB | 1983-08-16 | 85 |
| K790405 | ANCHOR BRAND COUNT-TAINER | MMK | 1979-03-26 | 28 |
Recalls
openFDA lists no recalls under a recalling firm named Anchor Products Co..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Anchor Implants , Ltd. (2 510(k)s)
- Anchor Innovation Medical (A.I.M.) (2 510(k)s)
- Anchor Brush Co., Inc. (1 510(k)s)
- Anchor Implant Systems, Inc. (1 510(k)s)
- Anchor Innovation Medical, Inc. (1 510(k)s)
- Anchor Medical Technologies (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Anchor Products Co.?
FDA lists 7 510(k) clearances under the applicant name “Anchor Products Co.” (first 1979, latest 2009), across 5 product codes in 2 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Anchor Products Co.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Anchor Products Co. is 85 days.
Which FDA product codes appear under Anchor Products Co.?
The most frequent FDA product codes under this applicant name are GCJ (Laparoscope, General & Plastic Surgery, 3); GAA (Needle, Aspiration And Injection, Disposable, 1); GAB (Needle, Suturing, Disposable, 1).
Next steps
- See all 7 Anchor Products Co. clearances with predicates and recalls
- Run predicate analysis for product code GCJ, Anchor Products Co.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.