uCentum™ comprehensive posterior system CS 3810-01

by Ulrich GmbH & Co. KG

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

1 closed

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04052536080854 UDI-DI	Date30 Jul 2016Listed	StatusListed GUDID: in commercial distribution

Recalls

1 recall · FDA

- Terminated Z-1126-2019 FDA Class II initiated 8 Mar 2019 on shared 510(k) K123717
Certain Torque Limiting Handles in the field are beyond their 3 year calibration life.

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: uCentum™ comprehensive posterior system
Generic Name: Bone-screw internal spinal fixation system connector
Model / Ref / Catalog: CS 3810-01

Primary DI / UDI-DI: 04052536080854
510(k) Number: K123717
FDA Product Code: MNI, NKB, MNH
GMDN Term: Bone-screw internal spinal fixation system connector

Device Class: Class II
Regulation Number: 888.3070
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization
MRI Safety: MR Conditional

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Properties

Single Use
Implantable
Prescription Use
Lot / Batch Number
Manufacturing Date

Other properties (9)

Sterile: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No
Expiration Date: No