Feeltech Co., Ltd. FDA Record
Feeltech Co., Ltd. has 0 FDA recalls, 2 inspections, 4 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Feeltech Co., Ltd." is on file.
- Latest inspection
- Sep 12, 2024 · NAI
- Latest 510(k)
- Oct 20, 2025
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 4 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 2 | Nov 14, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
FDA record by year
| Year | Inspections | OAI | Warning letters | Recall records | Class I |
|---|---|---|---|---|---|
| 2026 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 1 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2017 | 1 | 0 | 0 | 0 | 0 |
Recent FDA inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Sep 12, 2024 | Gunsan, Korea (The Republic Of) | Devices | No Action Indicated (NAI) | 3010462274 |
| Nov 8, 2017 | Gunsan, Korea (The Republic Of) | Devices | No Action Indicated (NAI) | 3010462274 |
- NAI
- No objectionable conditions or practices were found during the inspection.
- VAI
- Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
- OAI
- Regulatory and/or administrative actions are recommended.
FDA-inspected facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3010462274 | Gunsan, Korea (The Republic Of) | 2 | Sep 12, 2024 |
Recent 510(k) clearances
| K-Number | Device | Date |
|---|---|---|
| K251414 | Miracu Polydioxanone (PDO) Suture and Needle (MONO) | Oct 20, 2025 |
| K250107 | V-soft Line Barbed Surgical Suture (Various) | Oct 15, 2025 |
| K213010 | FEELject LDV (Low dead volume) syringe | May 31, 2023 |
| K172602 | Miracu | Nov 14, 2018 |
Feeltech Co., Ltd. and the FDA: common questions
Has Feeltech Co., Ltd. received an FDA warning letter?
No FDA warning letter addressed to the name "Feeltech Co., Ltd." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.
Has Feeltech Co., Ltd. received an FDA Form 483?
FDA has not published a Form 483 for "Feeltech Co., Ltd." in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Feeltech Co., Ltd.?
The most recent FDA inspection on file ended Sep 12, 2024 at Gunsan, Korea (The Republic Of) and was classified NAI. FDA has 2 inspections of Feeltech Co., Ltd. on file.
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