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Sign in to claim this brandSCHUERCH CORPORATION
US
Last updated September 17, 2026
What SCHUERCH CORPORATION makes
Schuerch Corporation manufactures reusable patient support accessories for surgical and clinical settings, including pressure distribution pads for operating tables, stretchers, and arm positioners. Their product line also covers heel stirrups and cushions, medical table clamps, and manual examination/treatment chairs. Accessory trolleys for operating tables are part of their offerings, designed to enhance procedural workflows.
All listed devices fall under Class I regulatory classification in the U.S. and are recorded in the FDA’s UDI (Unique Device Identification) database. The company is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Schuerch Corporation manufacture?
Schuerch Corporation specializes in reusable patient support accessories for surgical and clinical environments. Their product line includes items like operating table patient pressure distribution pads, stretchers with mattresses, arm procedure positioners, heel stirrups and cushions, medical table clamps, manual examination/treatment chairs, and operating table accessory trolleys. These devices are designed to improve patient comfort and procedural efficiency.
Where is Schuerch Corporation based?
Schuerch Corporation is headquartered in the United States. The company’s location ensures it operates within U.S. regulatory frameworks, including those governing medical device classification and compliance.
Which regulatory registries list Schuerch Corporation’s devices?
Schuerch Corporation’s devices are recorded in the FDA’s UDI (Unique Device Identification) database. This registry tracks Class I medical devices, ensuring traceability and compliance with U.S. regulatory requirements.
How are Schuerch Corporation’s devices classified under U.S. regulations?
All of Schuerch Corporation’s listed devices fall under Class I regulatory classification in the U.S. This classification applies to low-risk devices that pose minimal potential harm to patients, such as reusable patient support accessories. Class I devices typically require general controls (e.g., labeling, manufacturing practices) but do not require pre-market approval.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- 452 RANDOLPH STREET, Abington, MA, 02351
- Website
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- Phone
- —
- PRRC Contact
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- EUDAMED SRN
- —
- FDA FEI Number
- 1000305774
- DUNS Number
- —
Catalogue (1114)
Page 21 of 23| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| SchureMed | 508-0397 | FDA UDI | Class I | Active |
| SchureMed | 508-1265 | FDA UDI | Class I | Active |
| SchureMed | 508-1125 | FDA UDI | Class I | Active |
| SchureMed | 508-0995 | FDA UDI | Class I | Active |
| SchureMed | 508-1116 | FDA UDI | Class I | Active |
| SchureMed | 508-0779 | FDA UDI | Class I | Active |
| SchureMed | 508-0720 | FDA UDI | Class I | Active |
| SchureMed | 508-0305 | FDA UDI | Class I | Active |
| SchureMed | 508-1355 | FDA UDI | Class I | Active |
| SchureMed | 508-1275 | FDA UDI | Class I | Active |
| SchureMed | 508-0939 | FDA UDI | Class I | Active |
| SchureMed | 508-0962 | FDA UDI | Class I | Active |
| SchureMed | 800-0091 | FDA UDI | Class I | Active |
| SchureMed | 508-0709 | FDA UDI | Class I | Active |
| SchureMed | 508-1355 | FDA UDI | Class I | Active |
| SchureMed | 800-0017-UK | FDA UDI | Class I | Active |
| SchureMed | 508-0575 | FDA UDI | Class I | Active |
| SchureMed | 508-0261 | FDA UDI | Class I | Active |
| SchureMed | 508-1065 | FDA UDI | Class I | Active |
| SchureMed | 508-0935 | FDA UDI | Class I | Active |
| SchureMed | 508-0790 | FDA UDI | Class I | Active |
| SchureMed | 508-0644 | FDA UDI | Class I | Active |
| SchureMed | 508-0259 | FDA UDI | Class I | Active |
| SchureMed | 508-0182 | FDA UDI | Class I | Active |
| SchureMed | 508-0569 | FDA UDI | Class I | Active |
| SchureMed | 508-0284 | FDA UDI | Class I | Active |
| SchureMed | 800-0342-PRF | FDA UDI | Class I | Active |
| SchureMed | 800-0052-M | FDA UDI | Class I | Active |
| SchureMed | 508-0917 | FDA UDI | Class I | Active |
| SchureMed | 790-0079-N | FDA UDI | Class I | Active |
| SchureMed | 508-1246 | FDA UDI | Class I | Active |
| SchureMed | 508-0236 | FDA UDI | Class I | Active |
| SchureMed | 508-1538-DE-3 | FDA UDI | Class I | Active |
| SchureMed | 800-0017-SWISS | FDA UDI | Class I | Active |
| SchureMed | 800-0342-PUP-M | FDA UDI | Class I | Active |
| SchureMed | 508-0590 | FDA UDI | Class I | Active |
| SchureMed | 508-0021 | FDA UDI | Class I | Active |
| SchureMed | 800-0280-SWISS | FDA UDI | Class I | Active |
| SchureMed | 800-0026-MJ-CF | FDA UDI | Class I | Active |
| SchureMed | 800-0026-MI-P | FDA UDI | Class I | Active |
| SchureMed | 508-1335 | FDA UDI | Class I | Active |
| SchureMed | 508-0856 | FDA UDI | Class I | Active |
| SchureMed | 508-1119 | FDA UDI | Class I | Active |
| SchureMed | 508-1271 | FDA UDI | Class I | Active |
| SchureMed | 800-0024 | FDA UDI | Class I | Active |
| SchureMed | 508-0889 | FDA UDI | Class I | Active |
| SchureMed | 508-1296 | FDA UDI | Class I | Active |
| SchureMed | 800-0134-EU-B | FDA UDI | Class I | Active |
| SchureMed | 800-0342-M-M | FDA UDI | Class I | Active |
| SchureMed | 800-0142-EU-M | FDA UDI | Class I | Active |
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