Lab Industries, Inc. FDA Record
Lab Industries, Inc. has 0 FDA recalls, 0 inspections, 2 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Lab Industries, Inc." is on file.
- Latest 510(k)
- Apr 12, 1983
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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 | 2 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 0 | Nov 14, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Recent 510(k) clearances
| K-Number | Device | Date |
|---|---|---|
| K830745 | ADT DISPOSABLE SCALPEL W/STAINLESS STEEL | Apr 12, 1983 |
| K811771 | A.D.T. REUSABLE BONE MARROW NEEDLE | Jul 10, 1981 |
Lab Industries, Inc. and the FDA: common questions
Has Lab Industries, Inc. received an FDA warning letter?
No FDA warning letter addressed to the name "Lab Industries, Inc." 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 Lab Industries, Inc. received an FDA Form 483?
FDA has not published a Form 483 for "Lab Industries, Inc." in its reading room. FDA publishes some Form 483s, not all of them.
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