Memometal Technologies FDA Record
- Latest inspection NAI · Sep 26, 2012
- No warning letters matched by name
Memometal Technologies has 0 FDA recalls, 2 inspections, 10 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Memometal Technologies" is on file.
- Latest inspection
- Sep 26, 2012 · NAI
- Latest 510(k)
- Nov 17, 2011
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 11, 2026 (checked Nov 15, 2026, unchanged) | File dated Nov 10, 2026 | Current |
| 510(k) clearances | 10 | Nov 15, 2026 | File dated Nov 9, 2026 | Current |
| Inspections | 2 | Nov 15, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Reviewing Memometal Technologies as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.
Or check Memometal Technologies yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.
Recent FDA inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Sep 26, 2012 | Bruz, France | Devices | No Action Indicated (NAI) | 3004082045 |
| Oct 1, 2009 | Bruz, France | Devices | No Action Indicated (NAI) | 3004082045 |
- 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 3004082045 | Bruz, France | 2 | Sep 26, 2012 |
Recent 510(k) clearances
| K-Number | Device | Date |
|---|---|---|
| K112197 | MEMOMETAL INTRA-MEDULLARY BONE FASTENER | Nov 17, 2011 |
| K101930 | MEMOMETAL NAVIS BONE PLATING SYSTEM | Mar 15, 2011 |
| K102072 | MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE) | Nov 3, 2010 |
| K093820 | SUBFIX ARTHROEREISIS IMPLANT, MODELS SUT0065, SUT0080, SUT0090, SUT0100, SUT0115 | May 19, 2010 |
| K083447 | MEMOMETAL ANCHORAGE BONE PLATE SYSTEM, MODELS PLSS/PLSL, PLP10/PLP20/PLP30/PLP40/PLP50 | Feb 6, 2009 |
| K071941 | MEMOMETAL BONE ANCHORS | Dec 4, 2007 |
| K070598 | MEMOMETAL INTRA-MEDULLARY BONE FASTENER, MODELS SMART TOE / X-FUSE | Jul 26, 2007 |
| K070039 | MEMOMETAL FIXOS SCREWS | Mar 21, 2007 |
| K070031 | MEMOMETAL MEMORY STAPLES | Mar 19, 2007 |
| K070033 | MEMOMETAL VARISATION, MODELS AV26-08, AV26-10, AV90-08 AND AV90-10 | Mar 19, 2007 |
Memometal Technologies and the FDA: common questions
Has Memometal Technologies received an FDA warning letter?
No FDA warning letter addressed to the name "Memometal Technologies" 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 Memometal Technologies received an FDA Form 483?
FDA has not published a Form 483 for "Memometal Technologies" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Memometal Technologies?
The most recent FDA inspection on file ended Sep 26, 2012 at Bruz, France and was classified NAI. FDA has 2 inspections of Memometal Technologies on file.
Need more than this page shows? Ask about Memometal Technologies in Claude or ChatGPT and get every site's inspections, Form 483s, warning letters and import alerts, with a link to the FDA source for each record. The API key is free: no card.