LEVEL ONE CMFRecalls & reported problems across all models
KLS-Martin L.P. · 150 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
LEVEL ONE CMF models — page 2
150 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- LEVEL ONE CMF 25-772-11-91EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 25-774-11-91EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 25-872-06-91PLATE, BONE1 report
- LEVEL ONE CMF 25-873-09-91EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 25-873-47-91PLATE, BONE1 report
- LEVEL ONE CMF 25-875-05-91PLATE, BONE1 report
- LEVEL ONE CMF 25-882-11-91EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 25-882-15-91EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 25-882-19-91EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 25-883-09-91EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 25-886-09-91EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 50-174-03-91Prosthesis, condyle, mandibular, temporary1 report
- LEVEL ONE CMF 50-280-05-09PLATE, BONE1 report
- LEVEL ONE CMF 50-322-04-09PLATE, BONE1 report
- LEVEL ONE CMF 50-330-06-09PLATE, BONE1 report
- LEVEL ONE CMF 50-375-04-91PLATE, BONE1 report
- LEVEL ONE CMF 50-379-04-91PLATE, BONE1 report
- LEVEL ONE CMF 50-381-04-91PLATE, BONE1 report
- LEVEL ONE CMF 50-405-07-09PLATE, BONE1 report
- LEVEL ONE CMF 50-405-12-09PLATE, BONE1 report
- LEVEL ONE CMF 50-730-04-09EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 50-731-06-09EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 50-732-06-09EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 50-735-24-09EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 50-740-05-09EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 50-742-06-09PLATE, BONE1 report
- LEVEL ONE CMF 50-746-24-09EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 50-754-05-09EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 50-754-07-09EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 50-762-04-09EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 50-764-04-09EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 50-771-26-09EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 50-774-24-09EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 50-793-26-09EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 50-794-20-09EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 50-796-06-09EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 51-116-06-91EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 51-673-13-09EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 99-592-73-01EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 25-197-07-09PLATE, BONE1 report
- LEVEL ONE CMF 99-580-28-04SCREW, FIXATION, INTRAOSSEOUS1 report
- LEVEL ONE CMF 99-594-41-02PLATE, BONE1 report
- LEVEL ONE CMF 50-303-09-09PLATE, BONE1 report
- LEVEL ONE CMF 25-768-05-91PLATE, BONE1 report
- LEVEL ONE CMF 50-723-26-09PLATE, BONE1 report
- LEVEL ONE CMF 50-775-36-09EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 50-305-35-09EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- LEVEL ONE CMF 25-332-27-09PLATE, BONE1 report
- LEVEL ONE CMF 25-872-13-09PLATE, BONE1 report
- LEVEL ONE CMF 25-879-07-09Plate, fixation, bone1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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