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SynVitro Flush 15840125M

by CooperSurgical, Inc.

SynVitro Flush 15840125M is an IVF medium (FDA Class II; FDA product code MQL, Media, Reproductive) made by CooperSurgical, Inc., cleared under FDA 510(k) K003163 on 22 Mar 2001 and listed in FDA GUDID since 5 Feb 2026 (UDI-DI 00888937028607), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K003163

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00888937028607 UDI-DI Date5 Feb 2026ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK003163 Date22 Mar 2001DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K003163 decided 22 Mar 2001 Active
  • FDA GUDID UDI-DI 00888937028607 listed 5 Feb 2026 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K003163
  2. Listed FDA GUDID 00888937028607

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
SynVitro Flush
Generic name
IVF medium
Model / reference
15840125M
Primary DI / UDI-DI
00888937028607
510(k) Number
FDA product code
MQL
GMDN term
IVF medium
Device class
Class II
Regulation number
884.6180
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K003163)

Similar devices

Other devices filed under FDA product code MQL (Media, Reproductive).

Other devices from CooperSurgical, Inc.

See all devices from CooperSurgical, Inc. →

Properties

  • Supplied sterile
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)