Allied Hill Enterprises, Ltd. FDA Record
Allied Hill Enterprises, Ltd. has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Allied Hill Enterprises, Ltd." is on file.
- Latest 510(k)
- Dec 7, 2009
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 1 | 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 |
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Recent 510(k) clearances
| K-Number | Device | Date |
|---|---|---|
| K091198 | LIQUID FILLED RING TEETHER, MODEL 03807, LIQUID FILLED RING TEETHER, MODELS 1962005, 1962011, LIQUID… | Dec 7, 2009 |
Allied Hill Enterprises, Ltd. and the FDA: common questions
Has Allied Hill Enterprises, Ltd. received an FDA warning letter?
No FDA warning letter addressed to the name "Allied Hill Enterprises, 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 Allied Hill Enterprises, Ltd. received an FDA Form 483?
FDA has not published a Form 483 for "Allied Hill Enterprises, Ltd." in its reading room. FDA publishes some Form 483s, not all of them.
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