Merz Pharma GmbH & Co. Kgaa (contract manufacturer, Reinheim Hesse, DE): 2 new FDA device listings, incl. implant, dermal, for aesthetic use
Merz Pharma GmbH & Co. Kgaa (Reinheim Hesse, Delaware): 2 new FDA device listings, incl. implant, dermal, for aesthetic use. Its amount of 2 is above the median of 2 (69th percentile). Dated 113 days ago, it serves as a historical benchmark. Score 55/100. As of 2026-11-04, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).
Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
amount: 2 · 69th percentile of 2,709 DeviceEstablishmentPulse records · 1.0x the median
Free preview: all 14 published fields of this record are shown below. Locked: 39 related DE DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Merz Pharma GmbH & Co. Kgaa |
| Owner / operator | Merz Pharma GmbH & Co. KGaA |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Reinheim Hesse, DE |
| New listings | 2 |
| Devices | Implant, Dermal, For Aesthetic Use |
| Product codes | LMH |
| Device classes | Class III |
| Brand names | Belotero Volume (+) Lidocaine; Belotero Intense (+) Lidocaine |
| First new listing | 2026-05-28 |
| Latest new listing | 2026-07-15 |
| FDA registration number | 3006999111 |
| Registration expires | 2027-12-31 |
| amount percentile | 69th of 2,709 (median 2, 1.0x median) |
| Peer records CSV (40 DE records) | 🔒 Click to unlock → |
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL
- Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
- Record date: 2026-07-15
- Data refreshed: 2026-11-04
- Refunds on request within 14 days
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LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 04 Nov 2026 21:52:36 GMT
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Peer benchmark and outreach value: Merz Pharma GmbH & Co. Kgaa and 40 Delaware peers
- Delaware DeviceEstablishmentPulse records like this one: 40
- Merz Pharma GmbH & Co. Kgaa's amount: 69th percentile of 2,709 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Delaware peer: $8,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
55 / 100 Score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
What is the DeviceEstablishmentPulse record for Merz Pharma GmbH & Co. Kgaa in Reinheim Hesse, Delaware?
Merz Pharma GmbH & Co. Kgaa (Reinheim Hesse, DE), a contract manufacturer, added 2 FDA device listings between 2026-05-28 and 2026-07-15.
How does Merz Pharma GmbH & Co. Kgaa compare to other Delaware DeviceEstablishmentPulse records?
Its amount of 2 sits in the upper half (69th percentile) of 2,709 records; the median is 2. It is 113 days old; check the official source for later updates before acting.
Merz Pharma GmbH & Co. Kgaa vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Merz Pharma GmbH & Co. Kgaa | Reinheim Hesse, DE | 2 | 69th | 2026-07-15 |
| Tecomet Inc. | Wilmington, MA | 3 | 77th | 2026-10-15 |
| Bard Shannon Limited | Humacao, PR | 3 | 77th | 2026-10-14 |
| Orchid Orthopedic Solutions Oregon, Inc. | Oregon City, OR | 3 | 77th | 2026-10-05 |
Related records
- NGInstruments, Inc dba Avalign Cutting Instruments
- Millstone Medical Outsourcing LLC
- Tecomet Inc.
- Biopro, Inc.
- Bard Shannon Limited
- Cook Medical LLC
- Swiss-American CDMO,LLC
- Millstone Medical Outsourcing LLC.
- Karl Storz Endoscopy-America, Inc.
- Orchid Orthopedic Solutions Oregon, Inc.
- Philips Ultrasound LLC
- Zimmer, Inc.
DeviceEstablishmentPulse: Contract manufacturer DeviceEstablishmentPulse: Foreign establishment DeviceEstablishmentPulse: records in Delaware
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From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.