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Patterson® 71110618

by Patterson Dental Supply, Inc.

Patterson® 71110618 is a Class II device made by Patterson Dental Supply, Inc., cleared under FDA 510(k) K915618 on 25 Feb 1992 and listed in FDA GUDID since 8 May 2024 (UDI-DI D66207111061807), active as of 24 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 24 Oct 2026

Documents

510(k) K915618

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD66207111061807 UDI-DI Date8 May 2024ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k) from GUDID NumberK915618 Date25 Feb 1992IssuedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K915618 decided 25 Feb 1992 Active
  • FDA GUDID UDI-DI D66207111061807 listed 8 May 2024 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K915618
  2. Listed FDA GUDID D66207111061807

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Patterson®
Generic name
Composite dental impression material
Model / Ref / Catalog
71110618
Primary DI / UDI-DI
D66207111061807
510(k) Number
FDA product code
EMA
GMDN term
Composite dental impression material
Device class
Class II
Regulation number
872.3275
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code EMA (CEMENT, DENTAL).

Other devices from Patterson Dental Supply, Inc.

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Properties

  • Lot / batch number
  • Expiration date
Other properties (13, all answered No)