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iTClamp® 9200

by Innovative Trauma Care, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

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

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00854874004035 UDI-DI Date22 Nov 2016ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
iTClamp®
Generic Name
Wound clip, non-biodegradable
Model / Reference
9200
Primary DI / UDI-DI
00854874004035
510(k) Number
FDA Product Code
DXC
GMDN Term
Wound clip, non-biodegradable
Device Class
Class II
Regulation Number
870.4450
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Category: Wound clip, non-biodegradable

Cleared under the same submission (K150813)

Similar devices

Also classified as Wound clip, non-biodegradable.

Other devices from Innovative Trauma Care, Inc.

  • iTClamp® 9600

    Class II

  • iTClamp® 9100

    Class II

  • Itclamp 50

    Class II

  • iTClamp50

    Class II

  • Itclamp 50

    Class II

  • Itclamp 50

    Class II

Properties

  • Lot / Batch Number
  • Manufacturing Date

Other properties (12)

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