Croma-Pharma GmbH: PMA approval for saypha® ChiQ
Croma-Pharma GmbH (Leobendorf): PMA approval for saypha® ChiQ. Dated 145 days ago, it serves as a historical benchmark. Score 55/100. As of 2026-11-04, from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration).
Data as of · Compiled by Zalwin from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)
Free preview: all 8 published fields of this record are shown below. Locked: 499 related FdaApprovalPulse records and the 4-column CSV export.
| Field | Value |
|---|---|
| Sponsor | Croma-Pharma GmbH |
| Product | saypha® ChiQ |
| Generic / ingredient | Implant, dermal, for aesthetic use |
| Approval | PMA original approval (new class III device) |
| Application | P250021 |
| Decided | 2026-06-12 |
| Panel / class | General, Plastic Surgery |
| Sponsor location | Leobendorf |
| Peer records CSV (500 records) | 🔒 Click to unlock → |
| CRM-ready export with official source URLs | 🔒 Click to unlock → |
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CSV columns: Sponsor · Product · Approval · Decided · official source URL
- Source agency: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)
- Record date: 2026-06-12
- Data refreshed: 2026-11-04
- Refunds on request within 14 days
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LIVE PUBLIC DATA Source: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration) · Last refreshed: Wed, 04 Nov 2026 06:06:18 GMT
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55 / 100 Score
- A new product launch.
What is the FdaApprovalPulse record for Croma-Pharma GmbH in Leobendorf?
The FDA approved saypha® ChiQ (P250021) for Croma-Pharma GmbH on 2026-06-12: PMA original approval (new class iii device).
How does Croma-Pharma GmbH compare to other FdaApprovalPulse records?
It is 145 days old; check the official source for later updates before acting.
Croma-Pharma GmbH vs. top 3 peers
| Organization | Location | Record date |
|---|---|---|
| Croma-Pharma GmbH | Leobendorf | 2026-06-12 |
| Vivasure Medical , Ltd. | Galway | 2026-10-16 |
| Edwards Lifesciences, LLC | Irvine, CA | 2026-10-01 |
| Rejoni, Inc. | Bedford, MA | 2026-09-28 |
Related records
FdaApprovalPulse: PMA original approval (new class III device)
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From openFDA (PMA and Drugs@FDA). openFDA can lag FDA decisions by days to weeks. Drug supplement types follow the FDA submission class (labeling and REMS, manufacturing/CMC, efficacy, other). Company and product level only. Verify on FDA databases before relying on an approval.