# Symmetry Medical, Inc. - Manchester (contract manufacturer, Manchester, NH): 4 new FDA device listings, incl. orthopedic stereotaxic instrument

**Score:** 80/100

| Field | Value |
|---|---|
| Establishment | Symmetry Medical, Inc. - Manchester |
| Owner / operator | Tecomet |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Manchester, NH, US |
| New listings | 4 |
| Devices | Orthopedic Stereotaxic Instrument; Intervertebral Fusion Device With Bone Graft, Lumbar; Integrated Operating Table-Electromechanical Surgical System; Sterilization Wrap Containers, Trays, Cassettes & Other Accessories |
| Product codes | OLO, MAX, SIR, KCT |
| Device classes | Class II |
| Medical specialties | Neurology, Orthopedic, General, Plastic Surgery, General Hospital |
| Brand names | Medtronic Transportation / Sterilization Cassettes Expanded Nav Disc Prep instrument tray; OTT442 Six Instrument Sterilization Tray; OTT446 Webb Lite Scope Tray; Medtronic Transportation / Sterilization Cassettes IMPLANT TRAY PYRAMID +4; Medtronic Transportation / Sterilization Cassettes INSTRUMENT TRAY #1 PYRAMID +4; Medtronic Transportation / Sterilization Cassettes MRC 5.5 Module, Ti; Medtronic Transportation / Sterilization Cassettes IMPLANT TRAY, FULL THRD, SS; Medtronic Transportation / Sterilization Cassettes TRAY MRC IMPLANT |
| First new listing | 2026-08-21 |
| Latest new listing | 2026-08-23 |
| FDA registration number | 1221053 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-11-04T21:52:36.524Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.