Technical Products, Inc.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Technical Products, Inc.” (first 1995, latest 2002), across 5 product codes in 4 review panels. Median 510(k) review time under this name: 88 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 |
|---|---|---|---|
| MIB | Elastomer, Silicone Block | 2 | 2 |
| BTR | Tube, Tracheal (W/Wo Connector) | 1 | 1 |
| FEW | Catheter, Malecot | 1 | 1 |
| FTL | Mesh, Surgical, Polymeric | 1 | 1 |
| HXA | Prosthesis, Tendon, Passive | 1 | 1 |
Review panels
Most recent Technical Products, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K013321 | SILICONE TRACHEAL T-TUBES | BTR | 2002-06-04 | 242 |
| K973385 | OVAL SHAPES | HXA | 1997-12-05 | 88 |
| K973166 | DOW CORNING SILASTIC ELASTOMER Q7-4750 | MIB | 1997-11-21 | 88 |
| K971472 | SIL-TEC NONREINFORCED SHEETING, REINFORCED SHEETING, RADIOPAQUE SHEETING, REINFORCED RADIOPAQUE SHEETING, EXTRA FIRM GRA | FTL | 1997-07-01 | 69 |
| K971613 | SIL-TEC SMALL/LARGE BORE TUBING/SIL-TEC HIGH DUROMETER TUBING/SIL-TEC RADIOPAQUE TUBING | MIB | 1997-05-22 | 20 |
| K954116 | SILICONE MALECOT CATHETER WITH PEZZER/MUSHROOM TIP | FEW | 1995-11-06 | 109 |
Recalls
openFDA lists no recalls under a recalling firm named Technical Products, Inc..
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.
- Technical Medical Products, Inc. (3 510(k)s)
- Technical Resources, Inc. (3 510(k)s)
- Technical Associates of New England (1 510(k)s)
- Technical Devices For Medicine (1 510(k)s)
- Technical Enginuities Co. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Technical Products, Inc.?
FDA lists 6 510(k) clearances under the applicant name “Technical Products, Inc.” (first 1995, latest 2002), across 5 product codes in 4 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 Technical Products, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Technical Products, Inc. is 88 days.
Which FDA product codes appear under Technical Products, Inc.?
The most frequent FDA product codes under this applicant name are MIB (Elastomer, Silicone Block, 2); BTR (Tube, Tracheal (W/Wo Connector), 1); FEW (Catheter, Malecot, 1).
Next steps
- See all 6 Technical Products, Inc. clearances with predicates and recalls
- Run predicate analysis for product code MIB, Technical Products, Inc.'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.