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Inqu

by Isto Technologies, Inc. 2 variants

510(k) K071428

Inqu is a Class II device made by Isto Technologies, Inc., cleared under FDA 510(k) K071428 on 17 Sep 2007, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK071428 Date17 Sep 2007ClearedStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
MQV
Device class
Class II
Regulation
21 CFR Part 888.3045
Advisory committee
Orthopedic
FDA decision
SESE Substantially Equivalent

Related clearances

Clearances this device's FDA summary refers to, and clearances whose summaries refer to it: a citation, not a claim of equivalence.

Cited by

Source: 510k-lineage (choiben314), CC BY 4.0

Devices cleared under K071428

3 devices · FDA GUDID

Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.

Devices cleared under K071428
UDI-DISize and differences
InQu Granules 30cc IQSP-GR-130
Arteriocyte Medical Systems, Inc
IQSP-GR-130 / IQSP-GR-130M896IQSPGR1300 —On the market
InQu Matrix 5x10cm IQSP-MX-150
Arteriocyte Medical Systems, Inc
IQSP-MX-150 / IQSP-MX-150M896IQSPMX1500 —On the market
InQu Matrix 5x5cm IQSP-MX-125
Arteriocyte Medical Systems, Inc
IQSP-MX-125 / IQSP-MX-125M896IQSPMX1250 —On the market

Similar devices

Other devices filed under FDA product code MQV (Filler, Bone Void, Calcium Compound).

Other devices from Isto Technologies, Inc.

See all devices from Isto Technologies, Inc. →