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DemeCAPRONE MO1070136B6P

by DemeTECH Corp

DemeCAPRONE MO1070136B6P is a Class II device made by DemeTECH Corp, cleared under FDA 510(k) K130083 on 17 Jul 2013 and listed in FDA GUDID since 12 Jul 2019 (UDI-DI 10652927217190), 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) K130083

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 Number10652927217190 UDI-DI Date12 Jul 2019ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK130083 Date17 Jul 2013DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K130083 decided 17 Jul 2013 Active
  • FDA GUDID UDI-DI 10652927217190 listed 12 Jul 2019 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K130083
  2. Listed FDA GUDID 10652927217190

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
DemeCAPRONE
Generic name
Polyester suture, bioabsorbable, monofilament, non-antimicrobial
Model / reference
MO1070136B6P
Primary DI / UDI-DI
10652927217190
510(k) Number
FDA product code
GAM
GMDN term
Polyester suture, bioabsorbable, monofilament, non-antimicrobial
Device class
Class II
Regulation number
878.4493
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under Polyester suture, bioabsorbable, monofilament, non-antimicrobial.

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)