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Synthasome, Inc.

Last updated May 30, 2026

What Synthasome, Inc. makes

Synthasome, Inc. manufactures bioabsorbable synthetic polymer extra-gynaecological surgical mesh, including variants designed for specific surgical applications.

The company’s devices are classified as Class II under US regulations and are listed in the FDA’s 510(k) and UDI registries. The manufacturer is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country: US
Address: —
Website: synthasome.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: 858-490-9400
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 140697280

Catalogue (19)

Device	Model / Reference	Registries	Class	Status
X-Repair	Z009-30	FDA UDI	Class II	Active
X-RepairSL	Z020-20SL	FDA UDI	Class II	Active
X-Repair	Z008	FDA UDI	Class II	Active
X-RepairSL	Z021-160SL	FDA UDI	Class II	Active
X-RepairSL	Z024-80SL	FDA UDI	Class II	Active
X-RepairSL	Z020-160SL	FDA UDI	Class II	Active
X-RepairSL	Z022-80SL	FDA UDI	Class II	Active
X-Repair	Z010-30	FDA UDI	Class II	Active
X-RepairSL	Z021-80SL	FDA UDI	Class II	Active
X-Repair	Z009-25	FDA UDI	Class II	Active
X-Repair	Z009-35	FDA UDI	Class II	Active
X-RepairSL	Z020-80SL	FDA UDI	Class II	Active
X-Repair	Z009	FDA UDI	Class II	Active
X-Repair	Z010	FDA UDI	Class II	Active
X-RepairSL	Z021-20SL	FDA UDI	Class II	Active
X-Repair	Z010-35	FDA UDI	Class II	Active
X-Repair	K141394	FDA 510(k)	Class II	Active
X-Repairsl	K141499	FDA 510(k)	Class II	Active
Synthasome X-Repair	K083307	FDA 510(k)	Class II	Active

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